布劳综合征中肉芽肿性肝硬化的原始描述。 - Suppr

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An Original Description of Granulomatous Liver Cirrhosis in Blau Syndrome.

作者信息

Cropley Angela, Ashrafy Amir Hadji, Weltman Martin

机构信息

Nepean Hospital, Derby St, Kingswood, Sydney, Australia.

出版信息

Dig Dis Sci. 2019 Nov;64(11):3346-3349. doi: 10.1007/s10620-019-05682-8. Epub 2019 Jun 1.

DOI:10.1007/s10620-019-05682-8

PMID:31154542

Abstract

摘要

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本文引用的文献

A Case of Sporadic Blau Syndrome with an Uncommon Clinical Course.一例临床病程罕见的散发性布劳综合征病例。

Case Rep Rheumatol. 2018 Dec 30;2018:6292308. doi: 10.1155/2018/6292308. eCollection 2018.

Somatic NOD2 mosaicism in Blau syndrome.布劳综合征中的体细胞NOD2镶嵌现象。

J Allergy Clin Immunol. 2015 Aug;136(2):484-7.e2. doi: 10.1016/j.jaci.2014.12.1941. Epub 2015 Feb 25.

Hepatic sarcoidosis presenting as portal hypertension and liver cirrhosis: case report and review of the literature.以门静脉高压和肝硬化为表现的肝结节病：病例报告及文献复习

Case Rep Gastroenterol. 2012 Jan;6(1):183-9. doi: 10.1159/000338355. Epub 2012 Apr 18.

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.NOD2基因分型在布劳综合征和早发型结节病临床表型中的作用。

Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134.

Blau syndrome and related genetic disorders causing childhood arthritis.布劳综合征及导致儿童关节炎的相关遗传性疾病。

Curr Rheumatol Rep. 2005 Dec;7(6):427-33. doi: 10.1007/s11926-005-0046-3.

Caspase recruitment domain 15 mutations and rheumatic diseases.

Curr Opin Rheumatol. 2005 Sep;17(5):579-85. doi: 10.1097/01.bor.0000169362.61443.52.

Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions.伴有肉芽肿性肾损害的家族性肉芽肿性关节炎（布劳综合征）

J Pediatr. 1998 Sep;133(3):450-2. doi: 10.1016/s0022-3476(98)70286-0.

Liver involvement in familial granulomatous arthritis (Blau syndrome).肝脏受累于家族性肉芽肿性关节炎（布劳综合征）。

J Rheumatol. 1996 Feb;23(2):396-9.

Familial granulomatous arthritis, iritis, and rash.家族性肉芽肿性关节炎、虹膜炎和皮疹。

J Pediatr. 1985 Nov;107(5):689-93. doi: 10.1016/s0022-3476(85)80394-2.

Familial granulomatous synovitis, uveitis, and cranial neuropathies.家族性肉芽肿性滑膜炎、葡萄膜炎和颅神经病变。

Am J Med. 1985 May;78(5):801-4. doi: 10.1016/0002-9343(85)90286-4.

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