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中性粒细胞减少性不明原因发热和播散性肉芽肿病在急性淋巴细胞白血病患者中的表现。

Neutropenic fever of unknown origin and disseminated granulomatous disease in a patient with acute lymphoblastic leukemia.

机构信息

Hospital de Clinicas "José de San Martín", Universidad de Buenos Aires.

出版信息

Rev Fac Cien Med Univ Nac Cordoba. 2022 Sep 16;79(3):304-306. doi: 10.31053/1853.0605.v79.n3.34402.

DOI:10.31053/1853.0605.v79.n3.34402
PMID:36149078
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9590815/
Abstract

An 18-year-old male was admitted for his second induction chemotherapy treatment for an acute lymphoblastic leukaemia with cyclophosphamide, cytarabine, and mercaptopurine. He presented with high fever, abdominal pain, non-bloody diarrhoea, portal hypertension and leukopenia. Stool sample analysis, blood cultures and extensive work-up were negative. The only microbiologic evidence was the presence of cytomegalovirus DNA detected by PCR. A profound hypogammaglobulinemia was documented. Pathology material reported non-caseating granulomas in liver, bone marrow, duodenum and colon with negative cytomegalovirus immunostaining. What is your diagnosis?

摘要

一位 18 岁男性因急性淋巴细胞白血病接受环磷酰胺、阿糖胞苷和巯嘌呤的第二次诱导化疗而入院。他出现高热、腹痛、无血腹泻、门静脉高压和白细胞减少。粪便样本分析、血培养和广泛的检查均为阴性。唯一的微生物学证据是聚合酶链反应检测到巨细胞病毒 DNA 的存在。明确存在低丙种球蛋白血症。病理材料报告肝脏、骨髓、十二指肠和结肠存在非干酪性肉芽肿,巨细胞病毒免疫染色阴性。你的诊断是什么?

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63a6/9590815/7bf46d624dbc/1853-0605-79-3-304-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63a6/9590815/318160af4660/1853-0605-79-3-304-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63a6/9590815/7bf46d624dbc/1853-0605-79-3-304-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63a6/9590815/318160af4660/1853-0605-79-3-304-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63a6/9590815/7bf46d624dbc/1853-0605-79-3-304-g002.jpg

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本文引用的文献

1
Hypogammaglobulinemia in Adolescents and Young Adults with Acute Lymphoblastic Leukemia.青少年和青年急性淋巴细胞白血病患者的低丙种球蛋白血症。
J Adolesc Young Adult Oncol. 2020 Dec;9(6):687-692. doi: 10.1089/jayao.2020.0060. Epub 2020 Jul 13.
2
Mnemonic for the differential diagnosis of non-caseating granulomas.非干酪样肉芽肿鉴别诊断的记忆方法。
Sarcoidosis Vasc Diffuse Lung Dis. 2017;34(2):200-207. doi: 10.36141/svdld.v34i2.5674. Epub 2017 Apr 28.
3
Etiologies of consecutive series of non-necrotizing granulomas.连续性非坏死性肉芽肿的病因
Sarcoidosis Vasc Diffuse Lung Dis. 2017;34(2):115-121. doi: 10.36141/svdld.v34i2.5966. Epub 2017 Apr 28.
4
Clinical Manifestations, Diagnosis, and Treatment of Sarcoidosis.结节病的临床表现、诊断与治疗
Mayo Clin Proc Innov Qual Outcomes. 2019 Aug 2;3(3):358-375. doi: 10.1016/j.mayocpiqo.2019.04.006. eCollection 2019 Sep.
5
Differential diagnosis of granulomatous lung disease: clues and pitfalls: Number 4 in the Series "Pathology for the clinician" Edited by Peter Dorfmüller and Alberto Cavazza.肉芽肿性肺病的鉴别诊断:线索与陷阱:“临床医生病理学”系列之四,由彼得·多夫米勒和阿尔贝托·卡瓦扎编辑。
Eur Respir Rev. 2017 Aug 9;26(145). doi: 10.1183/16000617.0012-2017. Print 2017 Sep 30.
6
Granulomas in the gastrointestinal tract: deciphering the Pandora's box.胃肠道中的肉芽肿:开启潘多拉魔盒之谜
Virchows Arch. 2018 Jan;472(1):3-14. doi: 10.1007/s00428-017-2210-3. Epub 2017 Aug 4.
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Infectious optic neuropathies: a clinical update.感染性视神经病变:临床最新进展
Eye Brain. 2015 Sep 28;7:59-81. doi: 10.2147/EB.S69173. eCollection 2015.
8
Immunopathogenesis of granulomas in chronic autoinflammatory diseases.慢性自身炎症性疾病中肉芽肿的免疫发病机制。
Clin Transl Immunology. 2016 Dec 16;5(12):e118. doi: 10.1038/cti.2016.75. eCollection 2016 Dec.
9
A clinicopathological classification of granulomatous disorders.肉芽肿性疾病的临床病理分类
Postgrad Med J. 2000 Aug;76(898):457-65. doi: 10.1136/pmj.76.898.457.
10
Granulomatous infections: etiology and classification.肉芽肿性感染:病因与分类
Clin Infect Dis. 1996 Jul;23(1):146-58. doi: 10.1093/clinids/23.1.146.