The Paucity of Typical Pathology: An Autopsy Series of Typhus Group Rickettsiosis-Associated Hemophagocytic Lymphohistiocytosis

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Authors: Joshua Klinnert, Vasily Ovechko, Michelle Madden Felicella, April N. McDougal, Susie Muir, Patricia A. Crocquet-Valdes, David H. Walker, Blanton LS
Cited by: 1
References: 45

Abstract

. The disease, transmitted by rat and cat fleas, is endemic to seaboard regions worldwide. Recently, murine typhus has reemerged as an increasingly recognized cause of febrile illness in the United States, especially in Texas and Southern California. In addition to fever, manifestations often include headache, malaise, myalgias, and a maculopapular rash in approximately half of cases. Although usually considered a mild illness, when untreated, symptoms can last up to 3 weeks. Severe manifestations such as pneumonitis, acute kidney injury, and meningoencephalitis may occur. Historically, death has occurred in 0.4%, but in Southern California, the case fatality rate has been recently recorded at 1.8%. As murine typhus has reemerged, there have been growing reports that this infection has triggered hemophagocytic lymphohistiocytosis, a life-threatening hyperinflammatory syndrome. We herein report two fatal cases of hemophagocytic lymphohistiocytosis secondary to murine typhus. Autopsy revealed typhus group rickettsial antigen in tissues via immunohistochemistry, along with hemophagocytosis. Interestingly, the classic vascular and perivascular histopathologic findings associated with disseminated rickettsial infection were absent. These findings highlight an aberrant inflammatory cascade leading to hemophagocytic lymphohistiocytosis.

Fields of Study & Subjects

Autoimmune and Inflammatory Disorders Research Vector-borne infectious diseases T-cell and Retrovirus Studies

Publication details

Journal / source
Pathogens
Publisher
MDPI AG
Volume
15
Issue
2
Pages
230–230
Publication date
19 February 2026
Language
EN