Ali Mir Wasim, Rakshit Soumadip, Sarkar Atreyee, Mondal Md Karimulla, Datta Anup Kumar, Chatterjee Uttara
Department of Internal Medicine, IPGMER & SSKM Hospital, 242 Harish Mukherjee Road, Kolkata 700020, India.
Department of Pathology, IPGMER & SSKM Hospital, 242 Harish Mukherjee Road, Kolkata 700020, India.
Oxf Med Case Reports. 2024 Dec 10;2024(12):omae151. doi: 10.1093/omcr/omae151. eCollection 2024 Dec.
Enteric fever is one of the important causes of tropical fever with a prevalence of 11-21 million cases worldwide annually. It encompasses both typhoid and paratyphoid fever. Typhi is the causative organism for typhoid fever, manifesting as an uncomplicated febrile illness to life-threatening sepsis with multiorgan dysfunction. It is complicated by neuropsychiatric manifestation (2%-40%), gastrointestinal bleeding (10%), and intestinal perforation (1%-3%). Hemophagocytic Lymphohistiocytosis (HLH) is a rare complication of typhoid fever. Herein we report the case of a 24-year-old male from North-Eastern India, presenting with spikes of fever, altered behavior, a generalized rash, haematochezia, and hemophagocytes on bone marrow examination due to hemophagocytic lymphohistiocytosis secondary to complicated typhoid fever.
肠热症是热带发热的重要病因之一,全球每年患病率为1100万至2100万例。它包括伤寒和副伤寒热。伤寒杆菌是伤寒热的病原体,表现为从单纯发热性疾病到伴有多器官功能障碍的危及生命的败血症。其并发症包括神经精神表现(2% - 40%)、胃肠道出血(10%)和肠穿孔(1% - 3%)。噬血细胞性淋巴组织细胞增生症(HLH)是伤寒热的一种罕见并发症。在此,我们报告一例来自印度东北部的24岁男性病例,该患者因复杂型伤寒热继发噬血细胞性淋巴组织细胞增生症,出现发热高峰、行为改变、全身性皮疹、便血以及骨髓检查发现噬血细胞。