WordNet

inflammation of a vein (usually in the legs)

PrepTutorEJDIC

妨害する,じゃまする;(…を)妨害する《+『of』+『名』》
静脈炎

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1. 敗血症性骨盤血栓性静脈炎 septic pelvic thrombophlebitis
2. 化膿性（敗血症性）血栓性静脈炎 suppurative septic thrombophlebitis
3. 下肢の表在性血栓性静脈炎 superficial thrombophlebitis of the lower extremity
4. 下肢慢性静脈疾患の概要およびマネージメント overview and management of lower extremity chronic venous disease
5. カテーテル関連の上肢静脈血栓症 catheter related upper extremity venous thrombosis

English Journal

A case of concurrent pancreatic intraepithelial neoplasia and type 1 autoimmune pancreatitis with marked pancreatic duct dilatation.

Takano Y1, Nagahama M2, Yamamura E2, Maruoka N2, Yokomizo K3, Mizukami H3, Tanaka JI3, Ohike N4.
Clinical journal of gastroenterology.Clin J Gastroenterol.2016 Jun 28. [Epub ahead of print]
The case patient was a previously healthy 82-year-old male. Abdominal ultrasound during a medical check-up revealed a dilatation of the main pancreatic duct, and the patient was referred to our hospital for closer examination. Contrast-enhanced computed tomography (CT) revealed a low-density mass of
PMID 27351197

A case of IgG4-related mesenteritis.

Mori E1, Kamisawa T2, Tabata T1, Shibata S1, Chiba K1, Kuruma S1, Kuwata G1, Onishi T1, Fujiwara T1, Fujiwara J1, Arakawa T1, Momma K1, Koizumi K1, Matsumoto H3, Horiguchi S4.
Clinical journal of gastroenterology.Clin J Gastroenterol.2015 Dec;8(6):400-5. doi: 10.1007/s12328-015-0617-4. Epub 2015 Nov 18.
IgG4-related disease is a newly recognized fibroinflammatory condition characterized by tumefaction consisting of fibrosis with dense infiltration of IgG4-positive plasma cells; affecting various organs. A case of IgG4-related sclerosing mesenteritis is reported. A 64-year-old man was admitted to ou
PMID 26581887

A Patient with Autoimmune Pancreatitis Type 1 with Previously Known Lymphadenopathy, Both in the Context of IgG4-related Disease.

Alidjan FM1, Karim F2, Verdijk RM3, van Esser JW4, van Heerde MJ4.
The American journal of case reports.Am J Case Rep.2015 Nov 5;16:790-3.
BACKGROUND: Autoimmune pancreatitis (AIP) is an important clinical pathologic concept of IgG-4-related disease. AIP is a rare cause of chronic pancreatitis, characterized by a fibroinflammatory process by lymphoplasmacytic infiltrates, storiform fibrosis, obliterative phlebitis, and increased IgG4+
PMID 26537530

Japanese Journal

自己免疫性膵炎に先行して発症し，IgG4関連疾患と考えられた肝病変の一例

肝臓 57(5), 233-241, 2016
NAID 130005155232

帝王切開術でのヒアルロン酸ナトリウム／カルボキシメチルセルロース癒着防止吸収性バリアの使用経験

日本農村医学会雑誌 64(2), 125-130, 2015
NAID 130005092943

Autoimmune Pancreatitis with Primary Sclerosing Cholangitis-like Lesion

Acta medica Nagasakiensia 51(1), 35-38, 2006-03
NAID 110004308528

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IgG 陽性形質細胞の浸潤を認めたmulticentricCastleman病の1例

chioles, additionally surrounded by lymphocytes (B). Obstructive phlebitis was seen in parts (C). Immu-nohistochemically, infiltrating plasmacytes are highly positive for IgG4 (IgG4/IgG＞50%) (D). (Scale bar＝ A: 250 μm, B.C.D 67

Inflammatory myofibroblastic tumor versus IgG4-related ...

Obstructive phlebitis was observed in all of the IgG4-related sclerosing lesions, but in only 1/22 (4.5%) of IMT. The immunohistochemical expression of ALK was observed in 15/22 (68.2%) of IMT and 0/16 (0%) of IgG4-related sclerosing disease.