利妥昔单抗治疗后与腹泻和结肠病变相关的斑疹。

Q3 Medicine
European journal of case reports in internal medicine Pub Date : 2024-12-16 eCollection Date: 2024-01-01 DOI:10.12890/2024_005067
Yaqoub Alshatti, Meshaan Alenezi
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引用次数: 0

摘要

Malakoplakia是一种罕见的肉芽肿疾病,由于吞噬过程中溶酶体消化缺陷而发生,可模仿炎症性肠病(IBD)或恶性肿瘤,特别是免疫抑制患者。我们报告一例62岁男性igg4相关眼病患者,在接受利妥昔单抗治疗继发于膜增殖性肾小球肾炎的肾病综合征6周后出现持续腹泻和结肠病变。结肠镜检查显示全结肠炎伴粘膜颗粒状、血管模式丧失和小结节,初步怀疑为IBD。然而,结肠活检的组织学分析证实了malako斑与Michaelis-Gutmann体的存在,是这种情况的典型病理特征。患者经环丙沙星治疗2周,停用类固醇,症状完全缓解,组织学明显改善。随访期间,白色病灶数量和大小减少,未检出Michaelis-Gutmann小体。本病例强调了对免疫抑制患者的胃肠道病变进行广泛鉴别诊断的重要性,因为误诊可能导致免疫抑制治疗的不适当升级。认识斑疹的组织病理学特征,并将其与临床表现联系起来,对于及时诊断和有效治疗至关重要。本报告增加了关于利妥昔单抗相关斑疹病的有限文献,突出了其诊断和治疗的独特挑战。学习要点:Malakoplakia虽然罕见,但在非典型胃肠道病变的免疫抑制患者中应考虑,以防止误诊为炎症性肠病。组织病理学证据,如Michaelis-Gutmann体,是诊断斑疹的必要条件。及时停止免疫抑制剂和靶向抗生素治疗可导致临床和组织学解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malakoplakia Associated with Diarrhoea and Colonic Lesions After Rituximab Treatment.

Malakoplakia is a rare granulomatous condition that occurs due to defective lysosomal digestion during phagocytosis and can mimic inflammatory bowel disease (IBD) or malignancies, particularly in immunosuppressed patients. We report the case of a 62-year-old male with IgG4-related orbitopathy, who developed persistent diarrhoea and colonic lesions 6 weeks after receiving rituximab therapy for nephrotic syndrome secondary to membranoproliferative glomerulonephritis. Colonoscopy revealed pancolitis with mucosal granularity, loss of vascular pattern, and small nodules, raising initial suspicion for IBD. However, histological analysis of colonic biopsies confirmed malakoplakia with the presence of Michaelis-Gutmann bodies, pathognomonic for this condition. The patient was treated with ciprofloxacin for 2 weeks, and steroids were discontinued, leading to complete symptom resolution and significant histological improvement. During follow-up, the number and size of white lesions decreased, and no Michaelis-Gutmann bodies were detected. This case underscores the importance of maintaining a broad differential diagnosis for gastrointestinal lesions in immunosuppressed patients, as misdiagnosis can result in inappropriate escalation of immunosuppressive therapy. Recognizing the characteristic histopathology of malakoplakia and linking it with clinical findings are critical for timely diagnosis and effective management. This report adds to the limited literature on rituximab-associated malakoplakia, highlighting the unique challenges in its diagnosis and treatment.

Learning points: Malakoplakia, though rare, should be considered in immunosuppressed patients with atypical gastrointestinal lesions to prevent misdiagnosis as inflammatory bowel disease.Histopathological evidence, such as Michaelis-Gutmann bodies, is essential for diagnosing malakoplakia.Prompt discontinuation of immunosuppressants and targeted antibiotic therapy can lead to clinical and histological resolution.

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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
166
审稿时长
8 weeks
期刊介绍: The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.
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