The renal pathology of chediak-higashi disease: Usefulness of the urinary sediment as a confirmatory diagnostic test

Rafael Valenzuela, William A. Morningstar, Sudesh P. Makker

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

The presence of large cytoplasmic inclusions, thought to be abnormal lysosomes, seems to be the cytological hallmark of Chediak-Higashi disease in both humans and animals. This cell anomaly, originally reported in the leukocytes, is also present in various tissue cells, including kidneys. In the patient described, the abnormal inclusions were identified in renal cells of the urinary sediment. Thus, urine could provide a convenient source of diagnostic material in patients with Chediak-Higashi disease. In addition, the ultrastructure of these inclusions is described for the first time in human renal tissue.

Original languageEnglish (US)
Pages (from-to)230-232
Number of pages3
JournalHuman pathology
Volume8
Issue number2
DOIs
StatePublished - Mar 1977

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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