Khundadze Mamuka, Khurtsia Lali, Shulaia Natali, Kandelaki George
Medicine, David Tvildiani Medical University, Tbilisi, GEO.
Infectious Diseases, Vakhtang Bochorishvili Clinic, Tbilisi, GEO.
Cureus. 2024 Sep 25;16(9):e70156. doi: 10.7759/cureus.70156. eCollection 2024 Sep.
Langerhans cell histiocytosis (LCH) is a rare disorder predominantly affecting children and is characterized by a wide range of clinical presentations, which can make early identification of the disease difficult and result in the delay of appropriate treatment. The challenge is further compounded by the fact that diagnostic confirmation typically requires a biopsy of the bone or skin lesion, as well as immunohistochemical identification of molecular markers, which may not be readily available in all settings. This case report describes a two-year-old female who was initially misdiagnosed with infectious mononucleosis due to her non-specific presentation, highlighting the diagnostic challenges of LCH, particularly in resource-limited settings. The case highlights the importance of increasing clinical awareness of LCH and including this condition in differential diagnoses to ensure timely and appropriate management.
朗格汉斯细胞组织细胞增多症(LCH)是一种主要影响儿童的罕见疾病,其临床表现多种多样,这使得早期识别该疾病变得困难,并导致适当治疗的延迟。诊断通常需要对骨骼或皮肤病变进行活检以及对分子标志物进行免疫组化鉴定,而在所有情况下这些可能都无法轻易获得,这进一步加剧了挑战。本病例报告描述了一名两岁女性,因其非特异性表现最初被误诊为传染性单核细胞增多症,突出了LCH的诊断挑战,特别是在资源有限的环境中。该病例强调了提高对LCH的临床认识并将其纳入鉴别诊断以确保及时和适当管理的重要性。