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腹痛的罕见病因:厄尔德海姆-切斯特病。

A Rare Cause of Abdominal Pain: Erdheim-Chester Disease.

作者信息

Chatterjee Arjun, de la Fuente Jaime, Rech Karen L, Takahashi Naoki, Majumder Shounak

机构信息

Department of Internal Medicine, Cleveland Clinic, Cleveland, OH.

Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

出版信息

ACG Case Rep J. 2023 Jun 8;10(6):e01049. doi: 10.14309/crj.0000000000001049. eCollection 2023 Jun.

Abstract

A 65-year-old man presented with hematuria, night sweats, nausea, intermittent nonbloody diarrhea, and abdominal pain. Computed tomography angiogram with enterography showed retroperitoneal fibrosis surrounding both kidneys and ureters without any evidence of vascular obstruction or hydronephrosis. Laparoscopic biopsy demonstrated fibroadipose tissue involved by a subtle histiocytic infiltrate in a background of marked fibrosis, scattered lymphocytes, and plasma cells. The histiocytes strongly expressed CD163, Factor XIIIa, and . He was diagnosed with Erdheim-Chester disease, a rare histiocytic neoplasm uncommonly presenting with gastroenterological manifestations.

摘要

一名65岁男性出现血尿、盗汗、恶心、间歇性非血性腹泻和腹痛。计算机断层扫描血管造影术联合小肠造影显示双侧肾脏和输尿管周围有腹膜后纤维化,无血管阻塞或肾积水的证据。腹腔镜活检显示纤维脂肪组织有轻微组织细胞浸润,背景为明显纤维化、散在淋巴细胞和浆细胞。组织细胞强烈表达CD163、凝血因子XIIIa和 。他被诊断为 Erdheim-Chester 病,这是一种罕见的组织细胞肿瘤,很少表现为胃肠病学症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beb7/10249710/3e27ec9b8bf7/ac9-10-e01049-g001.jpg

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