Ez-Zaky Sara, Imrani Kaoutar, Boutatleb Joud, Moatassim Billah Nabil, Nassar Ittimade
Central Radiology Department, Ibn Sina Hospital, Mohammed V University, Rabat, Morocco.
Radiol Case Rep. 2024 Aug 16;19(11):4925-4928. doi: 10.1016/j.radcr.2024.07.086. eCollection 2024 Nov.
Dermatophytic disease is a rare condition, primarily described in North Africa. This orphan disease owes its name to Hadida and Schousboe. Although the pathophysiology remains poorly understood, it is often associated with immune deficiency and occurs in the context of high consanguinity, as in our case. We report the case of a 24-year-old man who presented a trichophytic disease due to Trichophyton rubrum, admitted for the appearance of numerous subcutaneous nodules, prompting consultation at our institution. This dermatophytic disease typically begins with recurrent ringworm of the scalp or involvement of hairless skin. The dermatophytes involved are of anthropophilic and zoophilic origin, with T. violaceum being the most frequently isolated species in ringworm cases in the Maghreb. To date, no treatment regimen has been established. However, improving immune status and using antifungals have delayed or prevented the visceral dissemination of the disease.
皮肤癣菌病是一种罕见疾病,主要在北非有相关描述。这种罕见病得名于哈迪达(Hadida)和舒斯博(Schousboe)。尽管其病理生理学仍未被充分理解,但它常与免疫缺陷相关,且如我们病例所示,多发生在近亲结婚的背景下。我们报告了一例24岁男性因红色毛癣菌引发皮肤癣菌病的病例,该患者因出现大量皮下结节入院,遂到我们机构就诊。这种皮肤癣菌病通常始于头皮反复出现癣或无毛皮肤受累。所涉及的皮肤癣菌源于嗜人型和嗜动物型,在马格里布地区,堇色毛癣菌是癣病例中最常分离出的菌种。迄今为止,尚未确立治疗方案。然而,改善免疫状态并使用抗真菌药物已延缓或预防了该疾病的内脏播散。