Malignant histiocytosis of lungs and chest wall: A case report of diagnostic conundrum and treatment challenges in a resource-poor setting

J. Ahmad, I. Inuwa, D. Haliru, I. Ibrahim
{"title":"Malignant histiocytosis of lungs and chest wall: A case report of diagnostic conundrum and treatment challenges in a resource-poor setting","authors":"J. Ahmad, I. Inuwa, D. Haliru, I. Ibrahim","doi":"10.4081/PJM.2018.9","DOIUrl":null,"url":null,"abstract":"Malignant histiocytosis is a rare condition with variable clinical presentation and prognosis. Its diagnosis requires high index of suspicion and further evaluation. Thus, it poses a diagnostic as well as management challenges especially in resource poor setting. The objective is to highlight the diagnosis and treatment challenges in the management of malignant histiocytosis so that physicians can diagnose it early and initiate appropriate treatment. Our patient is a 35-year-old man who presented with chest wall mass, dyspnoea and right cervical lymphadenopathy He was initially being evaluated for lymphoma. Biopsy of the lymph nodes was done twice in different hospitals and that of the chest wall mass done once. Histological diagnosis was arrived at with the aid of immunohistochemistry three months after his first presentation to the hospital. The patient was then commenced on chemotherapy and showed remarkable improvement on the short-term basis. Malignant histiocytosis is a rare disease laden with management challenges. Despite that, its diagnosis and treatment can be achieved even in resource poor setting with high index of suspicion, team work and good laboratory support.","PeriodicalId":430358,"journal":{"name":"Pyramid Journal of Medicine","volume":"86 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pyramid Journal of Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4081/PJM.2018.9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Malignant histiocytosis is a rare condition with variable clinical presentation and prognosis. Its diagnosis requires high index of suspicion and further evaluation. Thus, it poses a diagnostic as well as management challenges especially in resource poor setting. The objective is to highlight the diagnosis and treatment challenges in the management of malignant histiocytosis so that physicians can diagnose it early and initiate appropriate treatment. Our patient is a 35-year-old man who presented with chest wall mass, dyspnoea and right cervical lymphadenopathy He was initially being evaluated for lymphoma. Biopsy of the lymph nodes was done twice in different hospitals and that of the chest wall mass done once. Histological diagnosis was arrived at with the aid of immunohistochemistry three months after his first presentation to the hospital. The patient was then commenced on chemotherapy and showed remarkable improvement on the short-term basis. Malignant histiocytosis is a rare disease laden with management challenges. Despite that, its diagnosis and treatment can be achieved even in resource poor setting with high index of suspicion, team work and good laboratory support.
恶性组织细胞增生肺和胸壁:一个病例报告诊断难题和治疗挑战在资源贫乏的设置
恶性组织细胞增多症是一种罕见的疾病,临床表现和预后不一。其诊断需要高度的怀疑和进一步的评估。因此,它提出了诊断和管理的挑战,特别是在资源贫乏的环境。目的是强调恶性组织细胞增多症的诊断和治疗挑战,以便医生能够及早诊断并开始适当的治疗。我们的病人是一名35岁的男性,他表现为胸壁肿块,呼吸困难和右颈部淋巴结病变,他最初被评估为淋巴瘤。淋巴结活检在不同医院做了两次,胸壁肿块做了一次。在他第一次到医院就诊三个月后,通过免疫组织化学进行了组织学诊断。患者随后开始化疗,并在短期内表现出显着的改善。恶性组织细胞增多症是一种罕见的疾病,充满了管理挑战。尽管如此,即使在资源贫乏的环境中,通过高怀疑指数、团队合作和良好的实验室支持,也可以实现其诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信