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    A 68-year-old woman with a history of stage IIIA ovarian cancer in remission and pulmonary embolism on apixaban presented with recurrent episodic facial and neck swelling and facial flushing for the past 7 months (Figure 1). The patient reported that her symptoms were worse overnight when laying down to sleep and peaked when she woke up in the morning. The swelling improved gradually throughout the day, but never fully resolved. Bending forward exacerbated her facial and neck swelling and flushing.

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    Food protein-induced enterocolitis syndrome (FPIES) is a non–IgE-mediated gastrointestinal food allergy.1 The diagnosis of FPIES is primarily based on the clinical history, although its gastrointestinal symptoms are shared with many other conditions, complicating its differential diagnosis. An oral food challenge is indicated when the diagnosis is unclear, or to determine tolerance, with a potential risk to the patient.2

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    • In Current Issue! #Lymphocyte #transformation #test in the #diagnosis of adult #fish-induced #enterocolitis #syndrome https://t.co/KptPvw838k https://t.co/gEXmk268Py

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    Immune checkpoint inhibitors (ICIs) have entailed a radical change in the therapeutic landscape of multiple tumors. The ICIs enhance immunogenic activity against tumor cells through suppression of negative signaling over cytotoxic T cells. Nivolumab is a fully human immunoglobulin G4 antibody that blocks the interaction between programmed cell death protein-1 (PD-1) and its corresponding ligand. Interfering with physiological mechanisms of peripheral immune tolerance conducts intensified systemic immune response, which enhances antitumor activity, but also favors inflammation leading to a wide spectrum of immune-related adverse effects (irAEs).

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    Hypereosinophilic syndrome (HES) is a disease with diverse clinical presentations including cardiac, neurologic, cutaneous, or pulmonary manifestations.1 We present a case of a 64-year-old man, active smoker, with history of occasional cocaine use who visited the emergency department because of progressive darkening of fingertips for 2 weeks, accompanied by intense pain and aggravated by cold temperature. Physical examination showed ischemia of all fingertips bilaterally, with necrosis of left index, middle, and annular fingers and right middle finger (Figure 1, A), associated with decreased temperature and tenderness to palpation.

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    Summary This is a report on antithyroid arthritis syndrome (AAS) which is a rare adverse effect of antithyroid agents. AAS presents with severe symptoms including myalgia, arthralgia, arthritis, fever, and skin eruption due to the use of antithyroid agents. We encountered a 55-year-old woman with severe pain in the hand and forearm and arthralgia in multiple joints, including the knee, ankle, hand, and wrist on day 23 after initiation of methimazole (MMI) for Graves’ disease. Blood tests revealed elevated inflammation markers such as C-reactive protein and interleukin-6, and magnetic resonance imaging of the hands confirmed inflammation findings. After withdrawing MMI on day 25, symptoms showed a tendency toward improvement. Afterwards, inflammation markers also dropped to an almost normal range. In addition to the above findings, the absence of anti-neutrophil cytoplasmic antibodies and most vasculitis symptoms such as nephritis, skin, or pulmonary lesions led to the diagnosis of AAS.

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    Wolters Kluwer Health - 10 month(s) ago

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    • New in PAIN: a systematic review with meta-analysis of stress biomarkers in individuals with #fibromyalgia #syndrome. https://t.co/8f2qXJSk73

    • New in PAIN: a systematic review with meta-analysis of stress biomarkers in individuals with #fibromyalgia #syndrome. https://t.co/loDKT0jb0W