Sequential Complications of Hypercalcemia, Necrotizing Granulomatous Vasculitis, and Aplastic Anemia Occurring in One Patient with Angioimmunoblastic T-cell Lymphoma.

Autor:	Swarup S; Texas Tech University Health Sciences Center, Lubbock, Texas USA., Kopel J; Texas Tech University Health Sciences Center, Lubbock, Texas USA. Electronic address: jonathan.kopel@ttuhsc.edu., Thein KZ; Texas Tech University Health Sciences Center, Lubbock, Texas USA., Tarafdar K; Internal Medicine and Hematology-Oncology, Covenant Health System, Lubbock, Texas USA., Swarup K; University Medical Center, Lubbock, Texas USA., Thirumala S; Department of Pathology, Covenant Health System, Lubbock, Texas USA., Quick DP; Texas Tech University Health Sciences Center, Lubbock, Texas USA; Internal Medicine and Hematology-Oncology, Covenant Health System, Lubbock, Texas USA.
Jazyk:	angličtina
Zdroj:	The American journal of the medical sciences [Am J Med Sci] 2021 Mar; Vol. 361 (3), pp. 375-382. Date of Electronic Publication: 2020 Sep 03.
DOI:	10.1016/j.amjms.2020.09.003
Abstrakt:	In this case report of a patient with angioimmunoblastic T-cell lymphoma (AITL), we describe the occurrence of three sequential complications that have been reported uncommonly in this disease subtype. Firstly, the patient developed hypercalcemia due to elevated 1,25-didydroxyvitamin D. Although hypercalcemia in AITL is not rare (1-2% incidence), this case was unusual in that the complication developed when disease appeared stable and symptomatically, he was doing well otherwise. Hypercalcemia surprisingly resolved a few months later at a time when his disease appeared to be progressing. A year later, the patient presented with digital ischemia necessitating partial amputation of a finger. Pathological exam revealed granulomatous vasculitis of small and medium arterioles with infiltrating malignant T lymphocytes. Although skin manifestations are common in AITL, necrotizing granulomatous vasculitis with accompanying tumor cells leading to severe digital ischemia appears rare. Subsequently the patient developed profound pancytopenia with bone marrow confirming severe aplastic anemia. To our knowledge only one other case of aplastic anemia has been reported in a patient with AITL. We discuss the diagnostic and management considerations involved in this patient care and review similar reported cases. (Copyright © 2020. Published by Elsevier Inc.)
Databáze:	MEDLINE
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