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一名年轻男性肌肉侵袭性非霍奇金淋巴瘤表现为坏死性肌筋膜炎的罕见病例。

A Rare Case of Aggressive Non-Hodgkin's Lymphoma of the Muscle in a Young Male Presenting as Necrotizing Myofasciitis.

作者信息

Mehta Vaishali, Iqbal Javed, Akella Jagadish, Zaki Khawaja

机构信息

Pulmonary and Critical Care Medicine, Nassau University Medical Center, East Meadow, USA.

出版信息

Cureus. 2024 May 8;16(5):e59888. doi: 10.7759/cureus.59888. eCollection 2024 May.

Abstract

Non-Hodgkin's lymphoma (NHL) involving skeletal muscle is generally found to be a secondary metastasis and extremely rarely as a primary site of malignancy. Furthermore, in HIV patients, an increased incidence of lymphomas may be identified within the first six months of highly active antiretroviral therapy (HAART) initiation unmasked by immune reconstitution inflammatory syndrome (IRIS). We illustrate an extremely rare instance of NHL of the skeletal muscle in a young immunocompromised male with HIV/AIDS presenting as necrotizing myofasciitis complicated by compartment syndrome and hemodialysis-refractory type B lactic acidosis. A young Hispanic male with AIDS was admitted for acute left thigh pain and was soon found to have abscess formation with compartment syndrome requiring thigh fasciotomy. During the course of the ICU stay, the patient's clinical status acutely worsened with sepsis-induced multiorgan failure, including acute renal and acute liver failure requiring N-acetylcysteine and severe refractory metabolic acidosis requiring renal replacement therapy. Repeat imaging demonstrated diffuse myonecrosis. Left thigh muscle biopsy confirmed aggressive NHL of skeletal muscle. Despite months of arduous medical management in ICU, doxorubicin, vincristine, cyclophosphamide chemotherapy with concurrent high-dose prednisone for the vented patient, and intermittent curves of improvement, our patient succumbed to the nature of the disease and subsequently died from severe sepsis from the immunocompromised state. Interestingly, our patient's initial CD4 count was 1, which improved to 96 after five months of HAART, raising concerns for IRIS lymphoma. Given such rapid improvement with chemotherapy, the possibility of IRIS-related lymphoma, and the surprising dearth of data for chemotherapy use in critically ill patients on mechanical ventilation, more research is needed in these topics to better approach such complicated patients.

摘要

累及骨骼肌的非霍奇金淋巴瘤(NHL)通常被发现是继发性转移,极少作为原发恶性部位。此外,在艾滋病患者中,高效抗逆转录病毒治疗(HAART)开始后的头六个月内,可能会因免疫重建炎症综合征(IRIS)而发现淋巴瘤发病率增加。我们阐述了一例极为罕见的病例,一名患有艾滋病的免疫功能低下年轻男性发生骨骼肌NHL,表现为坏死性肌筋膜炎并伴有骨筋膜室综合征和血液透析难治性B型乳酸酸中毒。一名患有艾滋病的年轻西班牙裔男性因左大腿急性疼痛入院,很快被发现有脓肿形成并伴有骨筋膜室综合征,需要进行大腿筋膜切开术。在重症监护病房(ICU)住院期间,患者的临床状况急剧恶化,出现脓毒症诱导的多器官功能衰竭,包括急性肾和急性肝功能衰竭,需要使用N - 乙酰半胱氨酸,以及严重的难治性代谢性酸中毒,需要进行肾脏替代治疗。重复成像显示弥漫性肌坏死。左大腿肌肉活检证实为侵袭性骨骼肌NHL。尽管在ICU进行了数月的艰苦治疗,对通气患者使用多柔比星、长春新碱、环磷酰胺化疗并同时给予高剂量泼尼松,且病情有间歇性改善,但我们的患者最终还是因病死亡,随后死于免疫功能低下状态下的严重脓毒症。有趣的是,我们患者最初的CD4细胞计数为1,在接受HAART五个月后升至96,这引发了对IRIS相关淋巴瘤的担忧。鉴于化疗带来的如此迅速的改善、IRIS相关淋巴瘤的可能性,以及在机械通气的重症患者中使用化疗的数据惊人地匮乏,在这些主题上需要更多研究,以便更好地治疗此类复杂患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e16/11160345/e2874ca95c7e/cureus-0016-00000059888-i01.jpg

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