Haemophagocytic lymphohistiocytosis with collapsing lupus podocytopathy as an unusual manifestation of systemic lupus erythematosus with APOL1 double-risk alleles

Bhavin Chokshi; Vivette D’Agati; Lilian Bizzocchi; Beverly Johnson; Barbara Mendez; Belinda Jim

doi:10.1136/bcr-2018-227860

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Rare disease

CASE REPORT

Haemophagocytic lymphohistiocytosis with collapsing lupus podocytopathy as an unusual manifestation of systemic lupus erythematosus with APOL1 double-risk alleles

Authors

Bhavin Chokshi Division of Nephrology, Department of Medicine, Jacobi Medical Center at Albert Einstein College of Medicine, Bronx, New York, USA PubMed articles Google scholar articles
Vivette D’Agati Department of Pathology, Columbia University Medical Center, New York City, New York, USA PubMed articles Google scholar articles
Lilian Bizzocchi Division of Rheumatology, Department of Medicine, Jacobi Medical Center at Albert Einstein College of Medicine, Bronx, New York, USA PubMed articles Google scholar articles
Beverly Johnson Division of Rheumatology, Department of Medicine, Jacobi Medical Center at Albert Einstein College of Medicine, Bronx, New York, USA PubMed articles Google scholar articles
Barbara Mendez Division of Rheumatology, Department of Medicine, Jacobi Medical Center at Albert Einstein College of Medicine, Bronx, New York, USA PubMed articles Google scholar articles
Belinda Jim Division of Nephrology, Department of Medicine, Jacobi Medical Center at Albert Einstein College of Medicine, Bronx, New York, USA PubMed articles Google scholar articles

Correspondence to Dr Belinda Jim, belindajim286{at}gmail.com

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Citation

Chokshi B, D’Agati V, Bizzocchi L, et al

Haemophagocytic lymphohistiocytosis with collapsing lupus podocytopathy as an unusual manifestation of systemic lupus erythematosus with APOL1 double-risk alleles

BMJ Case Reports CP 2019;12:bcr-2018-227860.

Publication history

Accepted December 14, 2018
First published January 14, 2019.

Online issue publication

January 14, 2019

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