A case of unhealing skin ulcer with iatrogenic Cushing’s syndrome

Shrebash Paul, Hashiba Moontaha, Bikash Kumar Sarkar, Sanzida Khan, Majeda Khanam, Md Zobaer Ahmed, Ariful Basher
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Abstract

Cutaneous Leishmaniasis is a rare disease in South-East Asian countries like Bangladesh, often presenting as skin lesions, ulcers or granulomatous plaques on the arm or back. As the disease is uncommon, high index of suspicion is required for the diagnosis. We are presenting a case of cutaneous Leishmaniasis in a migrant Bangladeshi worker in the Kingdom of Saudi Arabia (KSA). The case was initially treated with antibiotics, emollients and systemic steroid for a long time. However, the disease progressed, and the patient developed features of iatrogenic Cushing syndrome. The diagnosis was confirmed with a skin biopsy, which revealed Leishmania parasite. He received treatment with Injectable liposomal Amphotericin B (LAmB) and oral Miltefosine with promising clinical response. Clinicians should be vigilant while treating non-healing ulcers, and consider CL when there is history of travelling to CL endemic areas J Bangladesh Coll Phys Surg 2023; 41(4): 334-337
医源性库欣综合征皮肤溃疡未愈合1例
皮肤利什曼病在孟加拉国等东南亚国家是一种罕见疾病,通常表现为手臂或背部的皮肤病变、溃疡或肉芽肿斑块。本病不常见,诊断时需高度怀疑。我们报告一例皮肤利什曼病,患者为沙特阿拉伯王国(KSA)的一名孟加拉国移民工人。该病例最初用抗生素、润肤剂和全身类固醇治疗了很长时间。然而,病情进展,患者出现医源性库欣综合征的特征。该诊断经皮肤活检证实,发现利什曼原虫。他接受注射两性霉素B (LAmB)脂质体和口服米替福辛治疗,临床反应良好。临床医生在治疗未愈合的溃疡时应保持警惕,并在有前往CL流行地区旅行史时考虑CL。41 (4): 334 - 337
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