Literature DB >> 16836570

Disseminated histoplasmosis presenting as thrombotic microangiopathy.

Denis M Dwyre1, Adam M Bell, Kathleen Siechen, Sanjeev Sethi, Thomas J Raife.   

Abstract

BACKGROUND: Thrombotic microangiopathies (TMA) are systemic vasoocclusive disorders associated with significant morbidity and mortality. Rapid and reliable diagnosis of TMA is critical. The diagnosis is complicated by a lack of objective and sensitive laboratory testing as well as multiple concurrent diseases, including infectious processes. CASE STUDY: We report two cases of disseminated histoplasmosis associated with TMA manifestations in renal transplant recipients, including one patient with histologically documented renal microthrombi; both patients were referred for plasma exchange. After the diagnosis of histoplasmosis, the treatment plan was changed to antifungal medications, reduced immuno-suppression, and supportive care, with progressive resolution of TMA manifestations.
CONCLUSION: TMA occurs in transplant populations in association with infections, medications, and other factors. Appropriate management includes recognition and treatment of possible etiological factors. Disseminated histoplasmosis should be considered in transplant patients presenting with TMA.

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Year:  2006        PMID: 16836570     DOI: 10.1111/j.1537-2995.2006.00873.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  2 in total

1.  Uncommon cause of fever in a pediatric kidney transplant recipient: Answers.

Authors:  Sidharth Kumar Sethi; Nikita Wadhwani; Pranaw Jha; Rajan Duggal; Reetesh Sharma; Shyam Bansal; Vijay Kher
Journal:  Pediatr Nephrol       Date:  2016-11-22       Impact factor: 3.714

Review 2.  Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease.

Authors:  Fedaey Abbas; Mohsen El Kossi; Jon Jin Kim; Ajay Sharma; Ahmed Halawa
Journal:  World J Transplant       Date:  2018-09-10
  2 in total

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