Interstitial Nephritis Associated with Glomerulonephritis in a Patient with Hashimoto's Disease and Idiopathic Portal Hypertension

10Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

A middle-aged woman with hypothyroidism, idiopathic portal hypertension and nephrotic syndrome is presented. This unusual clinical appearance could not be explained as SLE by serological examinations. Pathohistological examinations showed “Banti's liver”, Hashimoto's thyroiditis and diffuse proliferative glomerulonephritis with severe tubulo-interstitial nephritis. Immunohistochemical studies revealed IgA deposits in glomeruli. Electron microscopic study disclosed peculiar lucent areas of rarefaction with osmiophilic particles in tubular basement membranes. This tubulointerstitial nephritis was considered to be related to the immunological mechanism involving thyroid gland, liver and kidney disorders. This case thus had a clinically rare combination of these three. © 1992, The Japanese Society of Internal Medicine. All rights reserved.

Cite

CITATION STYLE

APA

Sasaki, H., Joh, K., Ohtsuka, I., Ohta, H., Ohhashi, T., Hoashi, S., … Isogai, Y. (1992). Interstitial Nephritis Associated with Glomerulonephritis in a Patient with Hashimoto’s Disease and Idiopathic Portal Hypertension. Internal Medicine, 31(5), 641–648. https://doi.org/10.2169/internalmedicine.31.641

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free