Drug reaction with eosinophilia and systemic symptoms syndrome with toxic epidermal necrolysis: Overlap in an HIV seropositive male with diffuse large “B” cell lymphoma – A rare case report

N. Bhatt, V. Belgaumkar, R. Chavan, N. Deshmukh
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Abstract

Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a severe drug-induced hypersensitivity reaction with varied presentations. We report a rare case of DRESS syndrome with toxic epidermal necrolysis (TEN) overlap associated with non-Hodgkin lymphoma (NHL). A 52-year-old male with retroviral disease presented with fever and diffuse skin peeling with mucosal erosions. The patient was on antitubercular therapy (ATT) for 1 month for suspected tubercular cervical lymphadenitis. He had facial edema, extensive skin tenderness, and denudation with a positive Nikolsky's sign, icterus, hepatosplenomegaly and multiple enlarged immobile nontender cervical, and axillary and inguinal lymph nodes. Investigations showed leukocytosis with hepatic and renal dysfunction. Skin histopathology was consistent with TEN. Based on Registry of Severe Cutaneous Adverse Reaction criteria, a diagnosis of ATT-induced DRESS with TEN overlap was made. Cervical lymph node biopsy and immunohistochemistry confirmed diffuse large B-cell NHL. ATT was withheld and the patient was treated with systemic steroids and assessed for initiation of chemotherapy. The profound immunological dysregulation in individuals with retroviral disease leads to varied clinical presentations, increasing the chances of diagnostic errors, and culminating in challenging scenarios. Therefore, seemingly innocuous symptoms and signs warrant thorough evaluation. Sound clinical acumen and prompt investigations for unusual causes such as malignancies can improve outcomes by aiding accurate diagnosis as well as avert untoward complications such as DRESS syndrome/TE.
嗜酸性粒细胞增多和全身症状综合征伴中毒性表皮坏死松解的药物反应:HIV血清阳性男性弥漫性大“B”细胞淋巴瘤的重叠——一例罕见病例报告
嗜酸性粒细胞增多和全身症状(DRESS)综合征的药物反应是一种严重的药物诱导的超敏反应,表现多种多样。我们报告了一例罕见的DRESS综合征,其中毒性表皮坏死松解症(TEN)重叠与非霍奇金淋巴瘤(NHL)相关。一名患有逆转录病毒疾病的52岁男性出现发烧和弥漫性皮肤剥落伴粘膜侵蚀。患者因疑似结核性颈淋巴结炎接受了为期1个月的抗结核治疗。他有面部水肿,广泛的皮肤压痛,伴有Nikolsky征阳性的剥脱,黄疸,肝脾肿大,多发性肿大,不动的非末端颈部、腋窝和腹股沟淋巴结肿大。调查显示白细胞增多伴肝肾功能障碍。皮肤组织病理学与TEN一致。根据严重皮肤不良反应登记标准,诊断ATT诱导的具有TEN重叠的DRESS。颈淋巴结活检和免疫组织化学证实弥漫性大B细胞NHL。ATT被扣留,患者接受全身类固醇治疗,并评估是否开始化疗。逆转录病毒疾病患者的严重免疫失调导致不同的临床表现,增加了诊断错误的机会,并最终导致具有挑战性的情况。因此,看似无害的症状和体征值得彻底评估。良好的临床敏锐性和对恶性肿瘤等异常原因的及时调查可以通过帮助准确诊断来改善结果,并避免DRESS综合征/TE等不良并发症。
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