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A 22-year-old woman presented with worsening vision loss and headaches. A diagnosis of acromegaly was confirmed after detection of an invasive pituitary macroadenoma and biochemical testing. Despite two attempts of surgical debulking of the tumour and administration of long-acting octreotide and cabergoline, growth hormone (GH) and insulin-like growth factor 1 (IGF-1) levels were uncontrolled. The patient experienced persistent headaches despite surgery, gamma knife radiation and ventriculoperitoneal shunt placement; she was then enrolled in the ACCESS trial (ClinicalTrials.gov identifier, NCT01995734). Pasireotide (Signifor; Signifor LAR) was initiated, which led to reduced GH and IGF-1 levels and resolution of her intractable headaches. This highlights the use of monthly pasireotide in resolving headaches and improved biochemical control in a patient with acromegaly. We postulate that the headaches improved due to an analgesic and/or anti-inflammatory effect mediated by somatostatin receptors targeted by pasireotide. This may represent an additional benefit of pasireotide and requires further investigation.
Pyoderma gangrenosum (PG) coexisting with Cogan's syndrome (CS) is uncommon, although cutaneous manifestations are known to develop in CS. A middle-aged white female patient had chronic relapsing PG requiring ciclosporin and prednisolone. Despite receiving optimal doses of ciclosporin and prednisolone, she developed acute vestibulo-auditory symptoms as a result of CS. Ciclosporin was switched to methotrexate and prednisolone was increased. However, she continued to develop acute scleritis, requiring methylprednisolone pulses, and still had further flares of PG. Her methotrexate was held off when she developed severe pneumonia and she then received a trial of intravenous immunoglobulins (IVIG) for her recurrent leg ulcers. Unfortunately, she failed to respond to IVIG. Her ulcers eventually responded to six doses of monthly intravenous cyclophosphamide induction. Although CS is not an antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis, we used pulse cyclophosphamide, based on the experience of cyclophosphamide efficacy in severe ANCA-associated vasculitis (AAV). Following induction, both diseases currently remain under control with azathioprine as maintenance treatment.
We report a case of severe lupus myocarditis with rapid, acute deterioration to cardiogenic shock and multiorgan failure, highlighting the importance of early identification and treatment of acute presentations in patients with systemic lupus erythematosus. A 31-year-old woman with previously diagnosed subacute cutaneous lupus erythematosus initially presented with abdominal pain and frank per-rectal bleeding. She deteriorated rapidly with type 1 respiratory failure and acute kidney injury requiring dialysis secondary to acute cardiac failure with a prolonged intensive care unit admission, over a month. A significantly elevated troponin, global hypokinesia on echocardiogram and normal coronary artery angiogram and cardiac MRI lead to the diagnosis of acute lupus myocarditis as the cause for the cardiogenic shock. She was treated with high-dose corticosteroids and eventually made a full recovery, with cardiac function returning to normal.
Hypoglycaemia is a well-documented 'stroke mimic'. The literature documents numerous case reports of patients presenting with focal neurological deficits subsequently attributed to hypoglycaemia. The significant majority of these cases are found in patients with pre-existing diabetes. We present case histories of two patients with no history of diabetes presenting to secondary care with reactive hypoglycaemia causing transient symptoms that were responsible for referral as a possible transient ischaemic attack. Although uncommon, metabolic disturbances such as hypoglycaemia should be considered in all patients presenting as a suspected stroke, even if they are not known to have diabetes.
Cognitive–behavioural therapy is a first-line treatment for post-traumatic stress disorder (PTSD), but it is difficult to implement in disaster settings. We report the case of an 80-year-old Japanese woman, who was diagnosed with PTSD after the 2011 triple disaster (earthquake, tsunami and nuclear plant accident) in Fukushima. Her recovery was greatly enhanced by the social support she received while living in Idobata-Nagaya community housing, established by Soma city in Fukushima, where residents could naturally discuss their traumatic experiences. Habituation to traumatic memories and processing of cognitive aspects of the psychological trauma, which are therapeutic mechanisms of trauma-focused psychotherapies, spontaneously occurred in this setting. The details of this case support the effectiveness of Idobata Nagaya as a provider of psychological first aid, an evidence-informed approach to assist children, adolescents, adults and families in the aftermath of a disaster.
Non-ketotic hyperglycaemia (NKH) is the most common metabolic cause of hemichorea-hemiballismus (HC-HB) and an often-reversible condition. A 68-year-old man presented to the emergency department with a severe hyperglycaemic episode and altered mental status. He was treated appropriately and discharged home after his blood glucose levels were normal with an improvement of mental status. Four weeks after the discharge, he returned with flailing movements of bilateral upper and lower limbs. MRI of the brain revealed hyperintensities of the bilateral putamen on T1-weighted imaging. The patient's symptoms improved with a combination of amantadine, clonazepam and tetrabenazine. Several hypotheses involving gemistocytes, calcification and petechial haemorrhage were proposed in support of imaging abnormalities in the striatum. Dopamine-depleting agents and neuroleptics are used in the treatment of chorea. It is recommended to try a dose of tetrabenazine in patients with NKH-induced HC-HB if no improvement is appreciated with initial treatment of glycaemic control.
A 45-year-old man presented 4 months after ABOi renal transplantation with febrile illness and bicytopenia necessitating cessation of mycophenolate mofetil. Dengue non-structural protein 1 antigen (NS1 Ag) test was positive. Lowest total leucocyte count was 3.1x109/L and platelet count was 14x109/L. As fever subsided, patient became tachypneic with abdominal distention and hypotension. Ultrasonographic evaluation revealed ascites, gall bladder wall oedema and bilateral pleural effusion consistent with dengue capillary leak syndrome. He developed massive ascites with abrupt weight gain of 4 kg within 24 hours and worsening renal dysfunction. Patient was deteriorating rapidly in spite of adequate supportive care and we gave a trial of intravenous immunoglobulin (0.5 g/kg/day) for 5 days. Patient improved from day 2, and by day 3, he became haemodynamically stable and recovered completely. Patient was stable at discharge and is on regular follow-up.
Description
Intercostal artery (ICA) pseudoaneurysm related to tube thoracostomy drainage procedure is not commonly encountered.1 But when haemothoraces develops due to pseudoaneurysms, they could be timely detected by CT with CT angiography (CTA) and treated via transarterial embolisation with mini coils.2 3 We report the case of a 9-year-old female child with medullobalstoma involving her brain and spine who was admitted for scheduled chemotherapy. She developed progressive dyspnoea (with oxygen saturation80%) and a right pleural effusion was noted. Subsequently, a right-sided thoracentesis with pigtail catheter insertion was performed. After thoracentesis, her respiratory pattern improved with decreased fluid drained from the pigtail catheter and thus the pigtail was removed. However, her shortness of breath with decreased breath sounds over the right lung fields recurred the next day. Repeat thoracentesis revealed bloody fluid. CT with CTA showed right haemothorax with active bleeding from the...
Publication date: Available online 19 June 2018
Source:Annals of Allergy, Asthma & Immunology
Author(s): Rebecca Scherzer, Mitchell H. Grayson
ObjectiveIt is a well-known fact that there is significant heterogeneity in the origins of asthma in adults and children. This article examines the roots of asthma across the ages including atopy, the role of the microbiome and viral infections, along with comorbidities/confounders such as obesity, aspirin-exacerbated respiratory disease (AERD), neutrophilic asthma, cigarette smoking and the possibility of an asthma-chronic obstructive pulmonary disease (COPD) overlap syndrome.Data SourcesData was taken from various scientific search engines including PubMed and Science Direct databases.Study SelectionsArticles that reviewed information on the origins of asthma in persons of all ages including different phenotypes and genotypes of asthma were used.ResultsAsthma is a common and complex disease whose origins are likely a combination of both genetic predisposition and environmental exposures. Factors such as the microbiome, other atopic disease, viral infections in young children, and other diagnoses such as obesity or AERD are important to consider when creating a treatment plan for patients.ConclusionAsthma is a disease that is often diagnosed in childhood but can present at any age. There is debate in the field as to whether asthma is one disease or several different diseases that include airway inflammation as a key finding. There are risk factors for disease in the environment and thru co-morbidities that likely play significant roles in both the origins of asthma, the development of symptoms, and the response to treatment. These factors are even more important as we look towards the future with the goal of personalized medicine.Response to Reviewers: ResponseWe appreciate the thoughtful comments about our manuscript from the Editors and Reviewers and have addressed each item below.
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Clinical Thyroidology, Volume 30, Issue 6, Page 269-272, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 284-286, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 251-254, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 277-279, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 255-257, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 246-250, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 258-262, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 273-276, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 263-265, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 280-283, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 266-268, June 2018.
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Clinical Thyroidology, Volume 30, Issue 6, Page 287-289, June 2018.
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Helicobacter, EarlyView.
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Helicobacter, EarlyView.
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Helicobacter, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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Clinical Otolaryngology, EarlyView.
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The Journal of Dermatology, EarlyView.
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The Journal of Dermatology, EarlyView.
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The Journal of Dermatology, EarlyView.
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The Journal of Dermatology, EarlyView.
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The Journal of Dermatology, EarlyView.
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The Journal of Dermatology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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International Forum of Allergy &Rhinology, EarlyView.
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Clinical &Experimental Allergy, EarlyView.
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Clinical &Experimental Allergy, EarlyView.
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Clinical &Experimental Allergy, EarlyView.
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Recently, immune checkpoint inhibitors have widely been used for the management of advanced melanoma. However, high-grade immune-related adverse events can occur, particularly with combination immunotherapy. W...
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Australasian Journal of Dermatology, EarlyView.
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Journal of the European Academy of Dermatology and Venereology, EarlyView.
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Journal of the European Academy of Dermatology and Venereology, EarlyView.
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Journal of the European Academy of Dermatology and Venereology, EarlyView.
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Journal of the European Academy of Dermatology and Venereology, EarlyView.
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Journal of the European Academy of Dermatology and Venereology, EarlyView.
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Allergy, EarlyView.
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Allergy, EarlyView.
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Allergy, EarlyView.
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Allergy, EarlyView.
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Allergy, EarlyView.
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Allergy, EarlyView.
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Allergy, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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International Journal of Dermatology, EarlyView.
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Publication date: Available online 18 June 2018
Source:European Annals of Otorhinolaryngology, Head and Neck Diseases
Author(s): S. Kallel, R. Kallel, S. Ayadi, A. Ghorbel
IntroductionWe report the first case of squamous cell carcinoma (SCC) of the thyroid gland coexisting with papillary thyroid carcinoma (PTC) and Hashimoto's thyroiditis and discuss various theories concerning the histogenesis of SCC of the thyroid gland and the optimal treatment strategy.Case reportA 54-year-old woman presented with an anterior neck mass measuring 4cm on clinical examination. Imaging showed a suspicious thyroid nodule invading the trachea. Total thyroidectomy with bilateral central lymph node resection was performed. Histological examination revealed tall cell variant of papillary thyroid carcinoma associated with SCC of the right lobe of the thyroid and Hashimoto's thyroiditis. Immunohistochemistry of the SCC showed positive staining for p53 and Ki67 and negative staining for thyroglobulin. The patient underwent adjuvant radioactive iodine therapy and radiotherapy. With postoperative follow-up of 24 months, the patient was in good health.DiscussionIn conclusion, the most probable origin of SCC in this case was malignant transformation from Hashimoto's thyroiditis following a phase of metaplasia. This immunohistological profile is associated with a better prognosis. Optimal treatment consists of extensive surgical resection of tumour tissuefollowed by radiotherapy.
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Journal of Cosmetic Dermatology, EarlyView.
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Journal of Cosmetic Dermatology, EarlyView.
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Journal of Cosmetic Dermatology, EarlyView.
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Journal of Cosmetic Dermatology, EarlyView.
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Journal of Cosmetic Dermatology, EarlyView.
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British Journal of Dermatology, EarlyView.
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British Journal of Dermatology, EarlyView.
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British Journal of Dermatology, EarlyView.
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British Journal of Dermatology, EarlyView.
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British Journal of Dermatology, EarlyView.
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British Journal of Dermatology, Volume 178, Issue 6, Page e397-e435, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1245-1245, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1243-1243, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page e440-e440, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page e459-e459, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page e439-e439, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1243-1245, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page e461-e461, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1233-1234, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1236-1237, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page e395-e395, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1240-1240, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1237-1238, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1239-1240, June 2018.
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British Journal of Dermatology, Volume 178, Issue 6, Page 1242-1242, June 2018.
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Sleep hygiene-related conditions are factors that affect the symptoms experienced by patients with obstructive sleep apnea (OSA). However, very few studies have investigated the association between sleep hygiene and sleep symptoms, especially in patients with mild or moderate OSA. This study evaluated the relationship between factors related to sleep hygiene and clinical symptoms in patients with mild to moderate OSA.
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Management of tracheal stenosis remains controversial. Endoscopic interventions commonly provide immediate relief of symptoms, but are associated with high recurrence rates. In contrast, high success rates have been reported in patients undergoing tracheal resection. However, well-defined indications and contraindications for tracheal resection are lacking and previous studies commonly ignore patient-related outcomes (e.g. dyspnoea). We aimed to evaluate the outcome of tracheal resection at our institution and identify risk factors for complications.
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Melnikoff and Bailey (M a...
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Casual readers of Vavvas et al.'s recent paper in PNAS (1) on the pharmacogenomics of age-related macular degeneration (AMD) may get the impression that the authors have made an important incremental advance based on a logical series of studies, each of which has been moving the science in the same...
https://ift.tt/2M4Y7P3
Vickers (1) offers little substantive criticism, but we address three items he mentions: (i) our choice of clinical endpoint, (ii) the potential for multiple-testing false positives, and (iii) the need for additional study. An important distinction of our study (2) is the use of neovascular AMD (nvAMD) as the endpoint....
https://ift.tt/2JRKwOr
Landy, Piazza, and Goodwin (LP&G) have codeveloped a seminal and indispensable new model of person perception (1, 2). While endorsing LP&G's model, we recently challenged one of its auxiliary hypotheses: the morality dominance hypothesis (MDH) (3). LP&G critiqued our studies, arguing that they merely qualify the MDH (4). We concur...
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EVOLUTION Correction for "Evolutionary history of carbon monoxide dehydrogenase/acetyl-CoA synthase, one of the oldest enzymatic complexes," by Panagiotis S. Adam, Guillaume Borrel, and Simonetta Gribaldo, which was first published January 22, 2018; 10.1073/pnas.1716667115 (Proc Natl Acad Sci USA 115:E1166–E1173). The authors wish to note the following: "We would like to...
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MICROBIOLOGY, BIOPHYSICS AND COMPUTATIONAL BIOLOGY Correction for "Structural basis for antibody recognition of the NANP repeats in Plasmodium falciparum circumsporozoite protein," by David Oyen, Jonathan L. Torres, Ulrike Wille-Reece, Christian F. Ockenhouse, Daniel Emerling, Jacob Glanville, Wayne Volkmuth, Yevel Flores-Garcia, Fidel Zavala, Andrew B. Ward, C. Richter King, and Ian...
https://ift.tt/2t7pPU2
A census of the biomass on Earth is key for understanding the structure and dynamics of the biosphere. However, a global, quantitative view of how the biomass of different taxa compare with one another is still lacking. Here, we assemble the overall biomass composition of the biosphere, establishing a census...
https://ift.tt/2M5SMqM
The identification and targeting of key molecular drivers of melanoma and breast and lung cancer have substantially improved their therapy. However, subtypes of each of these three common, lethal solid tumors lack identified molecular drivers, and are thus not amenable to targeted therapies. Here we show that pleckstrin homology domain-interacting...
https://ift.tt/2JRk4Ez
Antibiotic development is frequently plagued by the rapid emergence of drug resistance. However, assessing the risk of resistance development in the preclinical stage is difficult. Standard laboratory evolution approaches explore only a small fraction of the sequence space and fail to identify exceedingly rare resistance mutations and combinations thereof. Therefore,...
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Determining the structure of water adsorbed on solid surfaces is a notoriously difficult task and pushes the limits of experimental and theoretical techniques. Here, we follow the evolution of water agglomerates on Fe3O4(001); a complex mineral surface relevant in both modern technology and the natural environment. Strong OH–H2O bonds drive...
https://ift.tt/2tgfYvB
Experience induces de novo protein synthesis in the brain and protein synthesis is required for long-term memory. It is important to define the critical temporal window of protein synthesis and identify newly synthesized proteins required for memory formation. Using a behavioral paradigm that temporally separates the contextual exposure from the...
https://ift.tt/2t7pQr4
Histopathology based on spatial patterns of epithelial cells is the gold standard for clinical diagnoses and research in carcinomas; although known to be important, the tissue microenvironment is not readily used due to complex and subjective interpretation with existing tools. Here, we demonstrate accurate subtyping from molecular properties of epithelial...
https://ift.tt/2M4Y6dX
Activating mutations in the KIT or PDGFRA receptor tyrosine kinases are hallmarks of gastrointestinal stromal tumor (GIST). The biological underpinnings of recurrence following resection or disease progression beyond kinase mutation are poorly understood. Utilizing chromatin immunoprecipitation with sequencing of tumor samples and cell lines, we describe the enhancer landscape of...
https://ift.tt/2JOzRnu
The Balkans are considered the birthplace of mineral resource exploitation and metalworking in Europe. However, since knowledge of the timing and extent of metallurgy in southeastern Europe is largely constrained by discontinuous archaeological findings, the long-term environmental impact of past mineral resource exploitation is not fully understood. Here, we present...
https://ift.tt/2JONOBP
Skin is the largest organ of the body and represents the primary physical barrier between mammals and their external environment, yet the factors that govern skin microbial community composition among mammals are poorly understood. The objective of this research was to generate a skin microbiota baseline for members of the...
https://ift.tt/2M3m7lv
The Beclin 1–Vps34 complex, known as "mammalian class III PI3K," plays essential roles in membrane-mediated transport processes including autophagy and endosomal trafficking. Beclin 1 acts as a scaffolding molecule for the complex and readily transits from its metastable homodimeric state to interact with key modulators such as Atg14L or UVRAG...
https://ift.tt/2M5Zn4q
The mechanisms controlling the transcription of gene sets in specific regions of a plant embryo shortly after fertilization remain unknown. Previously, we showed that G564 mRNA, encoding a protein of unknown function, accumulates to high levels in the giant suspensor of both Scarlet Runner Bean (SRB) and Common Bean embryos,...
https://ift.tt/2JPBkdj
Microbial growth and division are fundamental processes relevant to many areas of life science. Of particular interest are homeostasis mechanisms, which buffer growth and division from accumulating fluctuations over multiple cycles. These mechanisms operate within single cells, possibly extending over several division cycles. However, all experimental studies to date have...
https://ift.tt/2tadXRw
AXL, a member of the TYRO3, AXL, and MERTK (TAM) receptor tyrosine kinase family, has been shown to play a role in the differentiation and activation of epidermal Langerhans cells (LCs). Here, we demonstrate that growth arrest-specific 6 (GAS6) protein, the predominant ligand of AXL, has no impact on LC...
https://ift.tt/2I3npe6
In adults, human hematopoietic stem and progenitor cells (HSPCs) reside in the bone marrow (BM) microenvironment. Our understanding of human hematopoiesis and the associated niche biology remains limited, due to human material accessibility and limits of existing in vitro culture models. The establishment of an in vitro BM system would...
https://ift.tt/2M4Y31L
Publication date: Available online 19 June 2018
Source:Journal of Allergy and Clinical Immunology
Author(s): Omar Tliba, Reynold A. Panettieri
Among patients with asthma, heterogeneity exists regarding the pattern of airway inflammation and response to treatment, prompting the necessity of recognizing specific phenotypes. Based on the analysis of inflammatory cell count in induced sputum, patients with asthma can be classified in four unique phenotypes; eosinophilic, neutrophilic, mixed granulocytic, and paucigranulocytic asthma (PGA). PGA is an asthma phenotype with no evidence of elevated numbers of eosinophils or neutrophils in sputum or blood, and in which anti-inflammatory therapies are ineffective in controlling symptoms. While under-investigated, PGA is the most common asthma phenotype in patients with stable asthma. However, PGA is sometimes underestimated due to the exclusive reliance on induced sputum cell count which is variable among cohorts of studies prompting the necessity of developing improved biomarkers. Importantly, investigators have reported that inhaled corticosteroids had limited effect on airway inflammatory markers in patients with PGA defining, therefore, PGA as a potentially "steroid-insensitive" phenotype that requires exploration of alternative therapies. PGA manifests as an uncoupling of airway obstruction from airway inflammation that can be driven by structural changes within the airways such as airway smooth muscle (ASM) tissue hypertrophy. Animal models provide evidence that processes evoking airway hyperresponsiveness and ASM thickening occur independent from inflammation and may be a consequence of a loss of negative homeostatic processes. Collectively, further understanding of PGA with focus on the characterization, prevalence, clinical significance and pathobiology derived from animal studies will likely provide precision therapies that will improve PGA clinical outcomes.
https://ift.tt/2tmAidT
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Publication date: Available online 19 June 2018
Source:Journal of Allergy and Clinical Immunology
Author(s): Donald A. Leopold, David Elkayam, John C. Messina, Colette Kosik-Gonzalez, Per G. Djupesland, Ramy A. Mahmoud
BackgroundChronic rhinosinusitis (CRS) is common and sometimes complicated by nasal polyps (NP). Corticosteroid nasal sprays are often unsatisfactory because they are ineffective at delivering medication to high/deep sites of inflammation.ObjectiveAssess whether an exhalation delivery system with fluticasone (EDS-FLU), capable of high/deep drug deposition, improves outcomes.MethodsPatients (N=323) ≥18 years with moderate-to-severe congestion and NP were randomized to twice-daily EDS-FLU (93, 186, or 372μg) or EDS-placebo for 24 weeks (16 double-blind [DB] plus 8 open-label [OL] when all received 372μg). Coprimary endpoints were change in nasal congestion/obstruction at 4 weeks and summed bilateral polyp grade at 16 weeks. Secondary endpoints included symptoms, polyp elimination, and functioning.ResultsEDS-FLU was superior on both co-primary endpoints (P < .001 vs EDS-placebo, all doses). Mean polyp grade improved continuously through week 24 (P < .009, all comparisons), with polyps eliminated on at least 1 side in ∼25% of patients at week 24 vs 8.7% with EDS-placebo (P≤0.014, all comparisons). Sino-nasal Outcomes Test (SNOT-22) scores also improved significantly versus EDS-placebo (-21.1 to -21.4 vs. -11.7 at week 16; P<0.05 all doses). At the end of DB, EDS-FLU (all doses) significantly improved all 4 defining disease symptoms. Most EDS-FLU patients (68%) reported "much" or "very much" improvement. The number of patients eligible for surgery decreased 62%-67%. The safety profile was similar to that reported in prior trials evaluating conventional corticosteroid nasal sprays in comparable populations.ConclusionEDS-FLU produces clinically and statistically significant improvement in all 4 diagnostically defining disease symptoms, polyp grade, and quality of life in CRSwNP.
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Publication date: Available online 18 June 2018
Source:Journal of Allergy and Clinical Immunology
Author(s): Irit Tirosh, Yasuhiro Yamazaki, Francesco Frugoni, Francesca A. Ververs, Eric J. Allenspach, Yu Zhang, Siobhan Burns, Waleed Al-Herz, Lenora Noroski, Jolan E. Walter, Andrew R. Gennery, Mirjam van der Burg, Luigi D. Notarangelo, Yu Nee Lee
BackgroundMutations in recombination-activating gene (RAG) 1 and RAG2 are associated with a broad range of clinical and immunologic phenotypes in human subjects.ObjectiveUsing a flow cytometry–based assay, we aimed to measure the recombinase activity of naturally occurring RAG2 mutant proteins and to correlate our results with the severity of the clinical and immunologic phenotype.MethodsAbelson virus–transformed Rag2−/− pro-B cells engineered to contain an inverted green fluorescent protein (GFP) cassette flanked by recombination signal sequences were transduced with retroviruses encoding either wild-type or 41 naturally occurring RAG2 variants. Bicistronic vectors were used to introduce compound heterozygous RAG2 variants. The percentage of GFP-expressing cells was evaluated by using flow cytometry, and high-throughput sequencing was used to analyze rearrangements at the endogenous immunoglobulin heavy chain (Igh) locus.ResultsThe RAG2 variants showed a wide range of recombination activity. Mutations associated with severe combined immunodeficiency and Omenn syndrome had significantly lower activity than those detected in patients with less severe clinical presentations. Four variants (P253R, F386L, N474S, and M502V) previously thought to be pathogenic were found to have wild-type levels of activity. Use of bicistronic vectors permitted us to assess more carefully the effect of compound heterozygous mutations, with good correlation between GFP expression and the number and diversity of Igh rearrangements.ConclusionsOur data support genotype-phenotype correlation in the setting of RAG2 deficiency. The assay described can be used to define the possible disease-causing role of novel RAG2 variants and might help predict the severity of the clinical phenotype.

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Publication date: Available online 18 June 2018
Source:Journal of Allergy and Clinical Immunology
Author(s): Dominika Polak, Christine Hafner, Peter Briza, Claudia Kitzmüller, Adelheid Elbe-Bürger, Nazanin Samadi, Maria Gschwandtner, Wolfgang Pfützner, Gerhard J. Zlabinger, Beatrice Jahn-Schmid, Barbara Bohle
BackgroundNeutrophils and allergen-specific T-cells accumulate in allergic late-phase reactions (LPR). Their presence is associated with severe inflammation. Cytokines like GM-CSF, IFN-γ, and IL-3, typically found in allergic LPR, have been proposed to convert neutrophils into antigen-presenting cells (APC).ObjectiveTo assess the antigen-processing and presenting capacity of neutrophils from allergic patients.MethodsNeutrophils were isolated from peripheral blood of birch pollen-allergic donors and stimulated with GM-CSF, IFN-γ, and IL-3. Viability and expression of HLA-DR, CD80, and CD86 were assessed by flow cytometry. HLA-DM expression was analysed by immunoblotting. Allergen-uptake was studied with fluorescence-labelled major birch pollen allergen Bet v 1. Bet v 1 was digested with neutrophilic endolysosomal extracts and resulting fragments were sequenced using mass spectrometry. Neutrophils were used as APC in co-culture experiments with autologous HLA-DR-restricted Bet v 1-specific T-cell clones reactive with epitopes in different regions of the allergen. In all experiments, monocytes were used for comparison. Fluids from suction blisters formed on top of LPR induced by intradermal allergen injection were assessed for HLA-DR-positive neutrophils by flow cytometry.ResultsThe cytokines significantly enhanced the survival, allergen uptake and expression of HLA-DM and HLA-DR of neutrophils. Neutrophils rapidly degraded Bet v 1 into fragments containing all relevant T-cell epitopes. Cytokine-activated, allergen-pulsed neutrophils induced proliferative and cytokine responses of Bet v 1-specific T-cells irrespective of epitope specificity confirming that they fully processed and presented the allergen. HLA-DR-positive neutrophils were detected in cutaneous allergic LPR.ConclusionNeutrophils may serve as APC for local allergen-specific effector T-cells in allergic LPR.
Publication date: Available online 18 June 2018
Source:Journal of Allergy and Clinical Immunology
Author(s): Juan Manuel Leyva-Castillo, Juhan Yoon, Raif S. Geha
BackgroundSerum IL-22 levels are elevated in atopic dermatitis (AD), which commonly precedes asthma in the atopic march. Epicutaneous (EC) sensitization in mice results in Th2-dominated skin inflammation that mimics AD, and sensitizes the airways for antigen challenge-induced allergic inflammation characterized by the presence of both eosinophils and neutrophils. EC sensitization results in elevated serum levels of IL-22.ObjectiveTo determine the role of IL-22 in antigen-driven airway allergic inflammation following inhalation challenge in EC sensitized mice.MethodsWild type (WT) and Il22-/- mice were EC sensitized or intraperitoneally (i.p.) immunized with ovalbumin (OVA) and intranasally challenged with antigen. OVA TCR-specific T cells were Th22 polarized in vitro. Airway inflammation, mRNA levels in the lungs and airway hyperresponsiveness (AHR) were examined.ResultsEC sensitization preferentially elicited an IL-22 response compared to i.p. immunization. Intranasal challenge of mice EC-sensitized with OVA elicited in the lungs Il22 mRNA expression, IL-22 production and accumulation of CD3+CD4+IL22+ T cells that co-expressed IL-17A and TNFα. EC-sensitized Il22-/- mice exhibited diminished eosinophil and neutrophil airway infiltration, and decreased AHR following intranasal OVA challenge. Production of IL-13, IL-17A and TNFα was normal, but IFNγ production was increased in lung cells from airway-challenged EC-sensitized Il22-/- mice. Intranasal instillation of IFNγ neutralizing antibody partially reversed the defect in eosinophil recruitment. WT recipients of Th22 polarized WT, but not IL-22 deficient, TCR-OVA specific T cells, which both secrete IL-17A and TNFα, developed neutrophil-dominated airway inflammation and AHR upon intranasal OVA challenge. Intranasal instillation of IL-22 with TNFα, but not IL-17A, elicited neutrophil-dominated airway inflammation, and AHR in WT mice, suggesting that the loss of IL-22 synergy with TNFα contributed to the defective recruitment of neutrophils into the airways of Il22-/- mice. TNFα, but not IL-22 blockade at the time of antigen inhalation challenge inhibited airway inflammation in EC sensitized miceConclusionEC sensitization promotes the generation of antigen-specific IL-22 producing T cells that promote airway inflammation and AHR following antigen challenge, suggesting that IL-22 plays an important role in the atopic march.





Publication date: September 2018
Source:International Journal of Pediatric Otorhinolaryngology, Volume 112
Author(s): Neelaysh Vukkadala, Danielle Perez, Sara Cabala, Cimeran Kapur, Dylan K. Chan
ObjectiveTo compare the English and non-English language performance of deaf or hard-of-hearing (DHH) children raised in homes where English was not the primary language to their typically hearing peers from similar language backgrounds.MethodsCase control study of bilingual DHH children with unilateral or bilateral non-fluctuating hearing loss defined as the most recent PTA between 26 and 70 dB in one or both ears. Typically hearing controls included bilingual siblings and children recruited from the General Pediatrics practice. Subjects completed the OWLS-II, a validated English language proficiency tool. The subject's parents completed the Child Behavioral Checklist, an assessment of problem behavior; the Student Oral Language Observation Matrix (SOLOM), an assessment of the child's non-English home language; and a study questionnaire on the child's medical, social, and language history.Results26 typically hearing controls, 15 children with bilateral hearing loss, and 18 children with unilateral hearing loss participated. The groups were similar in age, sex, insurance status, place of birth, age at arrival in the US, and maternal education status. Performance on the English language oral composite was significantly lower amongst the bilateral hearing loss group (BHL: 66.9, 95% CI [56.2–77.7]; UHL: 82.9, 95% CI [75.6–90.2]; NH: 84.4, 95% CI [79.5–89.3], p = 0.002). Performance on the SOLOM was significantly lower in bilateral hearing loss group. (BHL: 18.6, 95% CI [15.9–21.3]; UHL: 19.8, 95% CI [17.1–22.4]; NH: 22.3, 95% CI [20.6–24.0], p = 0.036).ConclusionsBilingual children with bilateral hearing loss are at increased risk for poor oral expressive and receptive language development. These children comprise a particularly vulnerable population who might benefit from additional focused interventions to support their language development.
https://ift.tt/2K24q5v
Publication date: August 2018
Source:Oral Oncology, Volume 83
Author(s): Pablo Ramos-García, Miguel Ángel González-Moles, Lucía González-Ruiz, Isabel Ruiz-Ávila, Ángela Ayén, José Antonio Gil-Montoya
ObjectivesTo evaluate the prognostic significance of cyclin D1 (CD1) overexpression in OSCC.Material and methodsWe searched studies published before August 2017 (Pubmed, Embase, Web of Science, Scopus). We evaluated the quality of the studies included (Quality in Prognosis Studies [QUIPS] tool). The impact of CD1 overexpression on overall survival and disease-free survival, T status, N status, stage, and histological degree was meta-analyzed. We analyzed heterogeneity among studies, conducted sensitivity analyses, analyzed small-study effects, and conducted subgroup analyses.Results31 studies (2942 patients) met inclusion criteria. Qualitative evaluation demonstrated that not all studies were performed with the same rigor, finding the greatest risk of bias in the study confounding domain. Quantitative evaluation showed that CD1 overexpression had a strong statistical association with worse overall survival (HR = 2.00, 95% CI = 1.59–2.51, p < 0.001), worse disease-free survival (HR = 1.46, 95% CI = 1.13–1.87, p = 0.003), higher T status (OR = 1.51, 95% CI = 1.07–2.13, p = 0.02), N+ status (OR = 2.16, 95% CI = 1.60–2.92, p < 0.001), advanced stage (OR = 1.44, 95% CI = 1.15–1.81, p = 0.002), and high histological grade (OR = 1.60, 95% CI = 1.12–2.29, p = 0.010). We observed heterogeneity in all parameters except for disease-free survival and clinical stage. We found effect of small studies on T and N status. The tonguel SCC subgroup showed the strongest association between CD1 overexpression and worse development. In addition, application of a cutoff point ≥10% tumor cells with nuclear CD1 expression maintained most of the significant associations reported.ConclusionsThese findings indicate that immunohistochemical assessment of CD1 overexpression may be useful as a prognostic biomarker for OSCC.
https://ift.tt/2yocbkL
Nasopharyngeal adenocarcinomas are rare tumours, and include neoplasms arising from the nasopharyngeal surface epithelium as well as those of minor salivary gland origin, each of which is distinct from the other. The former encompasses nasopharyngeal papillary adenocarcinoma (NPAC), also known as low grade NPAC and thyroid-like NPAC, an extremely unusual malignancy bearing histomorphological similarity to papillary thyroid carcinoma, and displaying indolent clinical behaviour. We report the case of a 41-year-old lady who developed NPAC as a second malignancy five-and-a-half years after being diagnosed and treated for a diffuse astrocytoma in the frontal lobe. In addition, we discuss the differential diagnosis, as well as raise certain pathogenetic considerations with regard to this unique neoplasm.