Garg Kapil Kumar, Singh Harpreet
Department of Internal Medicine, PGIMS, Rohtak, India.
Eur J Case Rep Intern Med. 2017 Mar 15;4(5):000605. doi: 10.12890/2017_000605. eCollection 2017.
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare and benign cause of lymphadenopathy and was first described in 1969. This disease commonly presents in children and young adults with supra-diaphragmatic lymphadenopathy mainly at cervical nodal sites, composed of a population of histiocytes. Since its description, over 400 cases have been described, but there are few reports in the literature on its association with lymphomas. This case report describes a case with co-existing SHML and anaplastic large cell lymphoma (ALCL). The diagnosis of SHML in our patient did not alter the clinical outcome and the patient responded well to treatment for ALCL. Clinicians should maintain a high index of suspicion in cases of infra-diaphragmatic SHML for the presence of occult lymphoma.
A rare presentation of sinus histiocytosis with massive lymphadenopathy (SHML) with anaplastic large cell lymphoma in the same lymph node at the same time is described.SHML has no proven clinical significance.A diagnosis of SHML in the presence of infra-diaphragmatic lymphadenopathy should raise a high index of suspicion for lymphoma.
伴巨大淋巴结病的窦性组织细胞增生症(SHML)是一种罕见的淋巴结病良性病因,于1969年首次被描述。该病常见于儿童和青年,主要表现为膈上淋巴结病,以颈部淋巴结部位为主,由一群组织细胞组成。自其被描述以来,已报道了400多例,但关于其与淋巴瘤关联的文献报道较少。本病例报告描述了1例同时存在SHML和间变性大细胞淋巴瘤(ALCL)的病例。我们患者的SHML诊断并未改变临床结局,且患者对ALCL治疗反应良好。对于膈下SHML病例,临床医生应高度怀疑隐匿性淋巴瘤的存在。
描述了1例罕见的同时在同一淋巴结出现伴巨大淋巴结病的窦性组织细胞增生症(SHML)和间变性大细胞淋巴瘤的病例。SHML尚无已证实的临床意义。在存在膈下淋巴结病的情况下诊断SHML应高度怀疑淋巴瘤。