Rare, yet emerging cause of graft dysfunction-ALECT 2 amyloidosis

Amyloidosis is characterized by pathological deposition of abnormal protein aggregates in various tissues, AL protein being the commonest. Amyloidosis derived from leukocyte cell-derived chemotaxin 2 (LECT2) is a recently recognized form of amyloidosis in the United States with predominant involveme...

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Veröffentlicht in:Indian journal of nephrology 2020-05, Vol.30 (3), p.204-206
Hauptverfasser: Singh, Kulwant, Sethi, Jasmine, Duggal, Rajan, Joshi, Kusum, Bains, Arjinder
Format: Artikel
Sprache:eng
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Zusammenfassung:Amyloidosis is characterized by pathological deposition of abnormal protein aggregates in various tissues, AL protein being the commonest. Amyloidosis derived from leukocyte cell-derived chemotaxin 2 (LECT2) is a recently recognized form of amyloidosis in the United States with predominant involvement of kidney and liver. We present a case of ALECT2 renal amyloid in a transplant recipient who presented with gradual worsening of graft function and subnephrotic proteinuria. To our knowledge, this is first case of LECT2 amyloidosis from Northern India in a transplant recipient. There is no effective therapy for amyloidosis derived from leukocyte cell-derived chemotaxin 2.
ISSN:0971-4065
1998-3662
DOI:10.4103/ijn.IJN_258_19