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2. Cutaneous oxalosis mimicking calcinosis cutis in a patient on peritoneal dialysis

Author

Audrey Rutherford, Travis Vandergriff, Arturo R. Dominguez, Hunter James Pyle, Stephanie Torres Rodriguez, and Shani Shastri

Subjects
oxalosis, Pathology, medicine.medical_specialty, medicine.medical_treatment, secondary hyperoxaluria, Lupus nephritis, Calcium oxalate, SLE, LN, lupus nephritis, Case Report, Dermatology, Secondary hyperoxaluria, End stage renal disease, Peritoneal dialysis, Calcinosis cutis, chemistry.chemical_compound, ESRD, end-stage renal disease, Biopsy, medicine, cutaneous oxalosis, lupus nephritis, secondary oxalosis, medicine.diagnostic_test, business.industry, food and beverages, medicine.disease, Connective tissue disease, chemistry, peritoneal dialysis, connective tissue disease, RL1-803, business, calcinosis cutis
Abstract

Oxalosis is the systemic accumulation of calcium oxalate in tissues throughout the body and can be of primary or secondary etiology. Extrarenal manifestations are rare but can include the cutaneous deposition of calcium oxalate. In this report, we discuss the case of a peritoneal dialysis patient, who presented with cutaneous papules and nodules mimicking calcinosis cutis. Subsequent biopsy resulted in a diagnosis of cutaneous oxalosis.

Published
2021

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