Rare case of immune mediated cutaneous leucoclastic vasculitis with pancytopenia in a rheumatoid arthritis patient with chronic cytomegalovirus infection

Rashmi Gupta Bajpai, Ayush Garg
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Abstract

Acute febrile illnesses with systemic involvement can present significant diagnostic and therapeutic challenges, particularly in patients with multiple comorbidities. This case report highlights a complex presentation of acute febrile illness with pancytopenia and immune-mediated cutaneous vasculitis in a patient with type II diabetes mellitus. A 52-year-old male with a known history of type II diabetes mellitus presented with fever, decreased oral intake, loose stools, oral ulcers, dysphagia, and rashes over the trunk and abdomen for four days. Upon admission to the ICU, extensive diagnostic evaluations were performed, revealing significant hematological, biochemical, and serological abnormalities. Imaging studies and histopathological examinations were conducted to further investigate the underlying etiology. Laboratory findings indicated pancytopenia, acute kidney injury, and hyperkalemia. Infectious disease workup was largely negative, except for a positive CMV IgG. Imaging studies revealed medical renal disease, and a skin punch biopsy confirmed cutaneous leukocytoclastic vasculitis. Bone marrow biopsy suggested bone marrow suppression. Multidisciplinary management, including dialysis, IV fluids, antibiotics, blood transfusions, steroids, and Ganciclovir, led to the patient’s gradual improvement and stabilization. The comprehensive diagnostic and therapeutic approach in this case underscores the importance of considering immune-mediated etiologies in patients with atypical presentations. Multidisciplinary collaboration was crucial in managing the multifaceted clinical condition of the patient. Early recognition and prompt multidisciplinary management are essential in similar cases. Extensive diagnostic evaluations should be performed to identify the underlying causes, and immune-mediated etiologies should be considered in complex presentations. Further research is recommended to explore optimal management strategies for such multifaceted conditions.  
慢性巨细胞病毒感染的类风湿性关节炎患者发生免疫介导的皮肤白细胞减少性血管炎并伴有全血细胞减少症的罕见病例
全身受累的急性发热性疾病会给诊断和治疗带来巨大挑战,尤其是对于患有多种并发症的患者。本病例报告重点介绍了一名 II 型糖尿病患者急性发热伴泛发性皮肤炎和免疫介导的皮肤血管炎的复杂表现。一名 52 岁的男性患者已知有 II 型糖尿病病史,表现为发热、进食减少、大便稀烂、口腔溃疡、吞咽困难以及躯干和腹部皮疹,已持续四天。入住重症监护室后,医生对其进行了广泛的诊断评估,发现其血液学、生化和血清学均有明显异常。为了进一步查明病因,对患者进行了影像学检查和组织病理学检查。实验室检查结果显示,患者出现全血细胞减少、急性肾损伤和高钾血症。除了 CMV IgG 阳性外,传染病检查结果基本为阴性。影像学检查发现了内科肾病,皮肤穿刺活检证实了皮肤白细胞坏死性血管炎。骨髓活检显示骨髓抑制。多学科治疗,包括透析、静脉输液、抗生素、输血、类固醇和更昔洛韦,使患者病情逐渐好转并趋于稳定。该病例的综合诊断和治疗方法强调了考虑非典型表现患者的免疫介导病因的重要性。多学科协作对于处理患者多方面的临床状况至关重要。在类似病例中,早期识别和及时的多学科管理至关重要。应进行广泛的诊断评估以确定潜在的病因,对于复杂的病例应考虑免疫介导的病因。建议进一步开展研究,探索针对此类多方面病症的最佳治疗策略。
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