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手部和足部二级残疾儿童的纯神经炎型麻风:1例罕见病例及文献综述

Pure Neuritic Leprosy In Children With Grade 2 Disability On Hands And Feet: A Rare Case And Literature Review.

作者信息

Gunawan Hendra, Ruchiatan Kartika, Puspitosari Diah, Hindritiani Reti, Usman Hermin Aminah, Widjaja Stephanie

机构信息

Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, Indonesia.

Department of Anatomical Pathology, Faculty of Medicine, Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, Indonesia.

出版信息

Int Med Case Rep J. 2025 Jan 28;18:195-203. doi: 10.2147/IMCRJ.S497894. eCollection 2025.

Abstract

Pure neuritic leprosy (PNL) is a rare clinical variant of leprosy, especially in children. This variant of leprosy only involves peripheral nerves without skin involvement or acid-fast bacilli (AFB) found on slit-skin smear examination. The challenging diagnosis and establishment of PNL due to the absence of skin lesions often lead to disability. A case of PNL with grade 2 disability of hands and feet in a 16-year-old boy was reported. The patient has been living in a leprosy-endemic area and has a history of contact with people who have symptoms of leprosy. On physical examination, there were finger contractures on both hands and feet, accompanied by bilateral ulnar, common peroneal, and posterior tibial nerve enlargement without any skin lesions. No AFB was found on the slit-skin smear examination. The diagnosis of PNL was established by the mononeuritis multiplex detected on the nerve conduction examination and the histopathological examine from the biopsy of the left ulnar nerve, which showed lymphocyte infiltration. The patient was treated with multidrug therapy for multibacillary leprosy and consulted with the Department of Physical Medicine and Rehabilitation and the Department of Orthopaedics and Traumatology for contracture management. Clinicians need to be aware of the signs and symptoms of PNL in order to avoid delays in diagnosis and treatment, as the diagnosis and establishment of PNL remain challenging.

摘要

纯神经炎型麻风(PNL)是麻风的一种罕见临床类型,在儿童中尤为少见。这种麻风类型仅累及周围神经,皮肤无受累,且在皮肤涂片检查中未发现抗酸杆菌(AFB)。由于缺乏皮肤损害,PNL的诊断颇具挑战性,常常导致残疾。本文报告了一例16岁男孩患有手脚二级残疾的PNL病例。该患者一直生活在麻风流行区,有与麻风症状患者接触的病史。体格检查发现双手和双脚有手指挛缩,双侧尺神经、腓总神经和胫后神经增粗,无任何皮肤损害。皮肤涂片检查未发现AFB。通过神经传导检查发现的多发性单神经炎以及对左侧尺神经活检的组织病理学检查显示淋巴细胞浸润,从而确诊为PNL。该患者接受了多菌型麻风的联合化疗,并就挛缩处理咨询了物理医学与康复科以及骨与创伤科。临床医生需要了解PNL的体征和症状,以避免诊断和治疗延误,因为PNL的诊断和确诊仍然具有挑战性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6ec/11786606/6ab84cdde710/IMCRJ-18-195-g0001.jpg

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