吞噬性淋巴组织细胞增多症合并弥散性组织浆菌病2例表现为短暂性全血细胞减少。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Novi Apriany, Usi Sukorini, Tri Ratnaningsih, Rizka Humardewayanti Asdie, Yanri Wijayanti Subronto, Susanna Hilda Hutajulu, Ibnu Purwanto, Mardiah Suci Hardianti
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引用次数: 0

摘要

由于反应性骨髓抑制引起的短暂性全血细胞减少症常发生在噬血细胞性淋巴组织细胞增多症(HLH)中,这是一种严重感染后过度免疫激活引起的综合征。我们报告了两例全血细胞减少症和弥散性组织浆菌病伴HLH的病例,最初怀疑是血液恶性肿瘤。我们的第一个病例记录了全血细胞减少症的改善与连续骨髓穿刺中荚膜组织浆清除之间的相关性。第二个病例表现为巨噬细胞吞噬大量组织浆,临床症状严重,随着全血细胞减少症的恢复,临床症状有所改善。这两个病例强调了对同时发生全血细胞减少和严重感染的病例进行全面和批判性分析的重要性,因为全血细胞减少可能是严重感染的基础,反之亦然。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two Cases of Hemophagocytic Lymphohistiocytosis Associated with Disseminated Histoplasmosis Presented with Transient Pancytopenia.

Transient pancytopenia due to reactive bone marrow suppression often occurs in hemophagocytic lymphohistiocytosis (HLH), a syndrome resulting from excessive immune activation following a severe infection. We reported two cases with pancytopenia and disseminated histoplasmosis accompanied by HLH, initially suspected to be blood malignancies. Our first case documented the relevance between the improvement of pancytopenia and the clearance of Histoplasma capsulatum in serial bone marrow aspirations. The second case showed immense Histoplasma engulfment by the macrophage in relation to a severe clinical condition, followed by improvement of clinical symptoms in accordance with the recovery of pancytopenia. These two cases highlighted the importance of comprehensive and critical analysis for cases with concurrent pancytopenia and severe infection, since it may be that the pancytopenia underlies the severe infection or vice versa.

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来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
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