WordNet

dangerous to health; characterized by progressive and uncontrolled growth (especially of a tumor)

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Orioli L, Boute C, Eloy P, De Wispelaere JF, De Coene B, Huang TD, Ausselet N, Delaere B.
Acta clinica Belgica.Acta Clin Belg.2015 Aug;70(4):291-4. doi: 10.1179/2295333715Y.0000000007.
We present the case of a 70-year-old non-diabetic patient who presented to the emergency department with unrelenting otalgia. A severe otitis externa (OE) and mastoiditis were treated with broad spectrum antibiotics and surgical drainage. No bacteria was isolated from surgical samples. Because the o
PMID 26284925

Woolnough K1, Wardlaw AJ2.
Immunology and allergy clinics of North America.Immunol Allergy Clin North Am.2015 Aug;35(3):477-92. doi: 10.1016/j.iac.2015.05.002. Epub 2015 Jun 18.
Lung disease associated with marked peripheral blood eosinophilia is unusual and nearly always clinically significant. Once recognized, it is generally easy to manage, albeit with long-term systemic corticosteroids. A failure to respond to oral steroids in the context of good compliance suggests a m
PMID 26209896

Factors that predict in-hospital mortality in eosinophilic granulomatosis with polyangiitis.

Hasegawa W1, Yamauchi Y, Yasunaga H, Sunohara M, Jo T, Matsui H, Fushimi K, Takami K, Nagase T.
Allergy.Allergy.2015 May;70(5):585-90. doi: 10.1111/all.12597. Epub 2015 Mar 5.
BACKGROUND: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic small-vessel vasculitis associated with asthma, eosinophilia, and necrotizing vasculitis. EGPA is potentially life-threatening and often involves peripheral neuropathies, peptic ulcers, cerebral vessel disease, and c
PMID 25703656

小林茂人
Otology Japan 23(3), 258-262, 2013
… 抗好中球細胞質抗体 (anti-neutrophil cytoplasm antibody: ANCA) に関連する血管炎 (ANCA-associated vasculitis: AAV) には、1) 顕微鏡的多発血管炎 (microscopic polyangiitis: MPA)、2) 多発血管炎性肉芽腫症 (granulomatosis with polyangiitis: GPA)(旧Wegener肉芽腫症)、3) 好酸球性多発血管炎性肉芽腫症 (eosinophilic granulomatosis with polyangiitis: EPGA)(Churg-Strauss症候群) がある。 …
NAID 130005065199

小野澤里衣子,坪井義夫,尾畑十善 [他],井上展聡,山田達夫,三宅勝久
臨床神経学 52(8), 567-570, 2012
Wegener肉芽腫症に合併したReversible posterior leukoencephalopathy syndrome（RPLS）を経験した．症例は45歳男性，約1年前にWegener肉芽腫症を発症し，免疫治療にて寛解状態であったが，治療開始10カ月後にRPLSを発症した．RPLSは，悪性高血圧や妊娠子癇，免疫抑制剤などの使用により発症する頭蓋内の可逆性脳症であるが，本症例は発症時，免 …
NAID 130004921057

Grade I Lymphomatoid Granulomatosis with Increased Uptake of [^<18>F] Fluorodeoxyglucose in Positron Emission Tomography : A Case Report

ARAI Hiromasa,OSHIRO Hisashi,YAMANAKA Sumitaka,YUKAWA Norio,WADA Nobuyuki,RINO Yasushi,WATANUKI Yuji,YAMANAKA Shoji,INAYAMA Yoshiaki,LEE Jin,NAKAYAMA Haruhiko,MASUDA Munetaka
Journal of clinical and experimental hematopathology 49(1), 39-44, 2009-05-01
… There are several reports describing [<SUP>18</SUP>F] fluorodeoxyglucose positron emission tomography (FDG-PET) findings in patients with lymphomatoid granulomatosis (LYG). … The patient was a 63-year-old Japanese male who underwent an FDG-PET/computed tomography (CT) scan in screening for a malignant lesion. …
NAID 10025683670