Atypical presentation of systemic lupus erythematosus in a 16-year-old boy: Case report.

Q3 Medicine Tunisie Medicale Pub Date : 2024-10-05 DOI:10.62438/tunismed.v102i10.5065
Hela Sahbani, Marwa Bahri, Emna Azza, Yosr Ben Abdennebi, Lamia Aissaoui
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Abstract

Introduction: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, characterized by a clear female predominance and a major clinical polymorphism. Some initial presentations, particularly in children and adolescents are exceptional. Our objective was to report an unusual initial presentation of SLE in a male adolescent.

Observation: We reported the case of a 16-year- old tunisian boy who was referred to the hematology emergency department because of a hemorrhagic syndrome. The evolution was marked by pancytopenia, prolonged fever and an anasarca with recurrent cardiac tamponade. Explorations concluded to SLE. The patient was started on pulse therapy of dexamethasone followed by immunoglobulin. He was also provided with pericardiocentesis with a favorable outcome.

Conclusion: SLE is characterized by clinical polymorphism, that's why diagnosis and management of complications could be difficult. SLE should be considered in differential diagnosis of many disorders, such as pancytopenia and cardiac tamponade.

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一名 16 岁男孩系统性红斑狼疮的非典型表现:病例报告。
导言系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,其特点是女性患者明显占多数,临床表现多态。有些患者,尤其是儿童和青少年患者的初始症状非常特殊。我们的目的是报告一名男性青少年系统性红斑狼疮不寻常的初始表现:我们报告的病例是一名 16 岁的突尼斯男孩,他因出血性综合征被转到血液科急诊。该病例的特征是泛发热、长期发热和伴有反复心脏填塞的哮喘。检查结果为系统性红斑狼疮。患者开始接受地塞米松脉冲治疗,随后注射免疫球蛋白。他还接受了心包穿刺术,结果良好:结论:系统性红斑狼疮的特点是临床多态性,因此并发症的诊断和处理可能会很困难。在许多疾病的鉴别诊断中都应考虑系统性红斑狼疮,如泛发性心肌炎和心脏填塞。
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来源期刊
Tunisie Medicale
Tunisie Medicale Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
72
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