Granulomatous Hypophysitis with Meningitis and Hypopituitarism
We report an unusual case of granulomatous hypophysitis in which visual impairment, meningitis and hypopituitarism in a 76-year-old female were associated with radiological evidence of a pituitary mass. The sellar lesion was indistinguishable from pituitary tumor on neuroimaging studies, but the rec...
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Veröffentlicht in: | Internal Medicine 1992, Vol.31(9), pp.1147-1150 |
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container_title | Internal Medicine |
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creator | YOSHIOKA, Mitsuaki YAMAKAWA, Norio SAITO, Hideaki YONEDA, Makoto NAKAYAMA, Toru KUROKI, Mizuo TSUCHIDA, Tadashi SEKIYA, Masao |
description | We report an unusual case of granulomatous hypophysitis in which visual impairment, meningitis and hypopituitarism in a 76-year-old female were associated with radiological evidence of a pituitary mass. The sellar lesion was indistinguishable from pituitary tumor on neuroimaging studies, but the recovery of visual acuity and visual field abnormalities together with the improvement of pituitary function after steroid administration indicated that the mass lesion was due to an inflammatory disease of the pituitary gland. The pituitary tissue obtained by transsphenoidal hypophysectomy revealed granulomatous inflammatory cell infiltration with epithelioid cells and scattered multinucleated giant cells. Although a causal relationship with meningitis was not ascertained, possible exposure of the CSF space to the autoimmune inflammatory process of the pituitary gland was likely in view of the positive pituitary antibody reaction and radiological evidence of suprasellar extension. This entity should be considered when evaluating patients with a pituitary mass, hypopituitarism and meningitis. (Internal Medicine 31 : 1147-1150, 1992) |
doi_str_mv | 10.2169/internalmedicine.31.1147 |
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The sellar lesion was indistinguishable from pituitary tumor on neuroimaging studies, but the recovery of visual acuity and visual field abnormalities together with the improvement of pituitary function after steroid administration indicated that the mass lesion was due to an inflammatory disease of the pituitary gland. The pituitary tissue obtained by transsphenoidal hypophysectomy revealed granulomatous inflammatory cell infiltration with epithelioid cells and scattered multinucleated giant cells. Although a causal relationship with meningitis was not ascertained, possible exposure of the CSF space to the autoimmune inflammatory process of the pituitary gland was likely in view of the positive pituitary antibody reaction and radiological evidence of suprasellar extension. This entity should be considered when evaluating patients with a pituitary mass, hypopituitarism and meningitis. 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Med.</addtitle><description>We report an unusual case of granulomatous hypophysitis in which visual impairment, meningitis and hypopituitarism in a 76-year-old female were associated with radiological evidence of a pituitary mass. The sellar lesion was indistinguishable from pituitary tumor on neuroimaging studies, but the recovery of visual acuity and visual field abnormalities together with the improvement of pituitary function after steroid administration indicated that the mass lesion was due to an inflammatory disease of the pituitary gland. The pituitary tissue obtained by transsphenoidal hypophysectomy revealed granulomatous inflammatory cell infiltration with epithelioid cells and scattered multinucleated giant cells. Although a causal relationship with meningitis was not ascertained, possible exposure of the CSF space to the autoimmune inflammatory process of the pituitary gland was likely in view of the positive pituitary antibody reaction and radiological evidence of suprasellar extension. This entity should be considered when evaluating patients with a pituitary mass, hypopituitarism and meningitis. (Internal Medicine 31 : 1147-1150, 1992)</description><subject>Aged</subject><subject>Female</subject><subject>Granuloma, Giant Cell - complications</subject><subject>Granuloma, Giant Cell - surgery</subject><subject>hemianopsia</subject><subject>Hemianopsia - etiology</subject><subject>Humans</subject><subject>hypopituitarism</subject><subject>Hypopituitarism - etiology</subject><subject>Hypopituitarism - surgery</subject><subject>Meningitis - etiology</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplUF1LwzAUDaLMOf0JQp9868xN2qZ5EWToJkxE0OeQpumW0aYzSZH9e1srE_TlXi7n63IQigDPCWT81tignZV1o0ujjNVzCnOAhJ2gKdCEx4zQ9BRNMYc8Jv04Rxfe7zCmOeNkgiaQEGAkn6K7pZO2q9tGhrbz0eqwb_fbgzfB-OjThG30rK2xm-9b2nIkmNCZIJ3xzSU6q2Tt9dXPnqH3x4e3xSpevyyfFvfrWKUYh1hnmpECEgBgiQTNuGSFriitsIIqzRXGikvIAedlhXGiWJGwNC3SskwYYxWdoZvRd-_aj077IBrjla5raXX_t2CUcJKxrCfmI1G51nunK7F3ppHuIACLoTrxtzpBQQzV9dLrn4yu6MFf4dhVj7-O-M4HudFHXLpgVK3_GQPnZDDn4xgyjly1lU5oS78A5IiOMQ</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>YOSHIOKA, Mitsuaki</creator><creator>YAMAKAWA, Norio</creator><creator>SAITO, Hideaki</creator><creator>YONEDA, Makoto</creator><creator>NAKAYAMA, Toru</creator><creator>KUROKI, Mizuo</creator><creator>TSUCHIDA, Tadashi</creator><creator>SEKIYA, Masao</creator><general>The Japanese Society of Internal Medicine</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1992</creationdate><title>Granulomatous Hypophysitis with Meningitis and Hypopituitarism</title><author>YOSHIOKA, Mitsuaki ; YAMAKAWA, Norio ; SAITO, Hideaki ; YONEDA, Makoto ; NAKAYAMA, Toru ; KUROKI, Mizuo ; TSUCHIDA, Tadashi ; SEKIYA, Masao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-e6e72b1411174a1e79a7bef33f0c1f58c00c9a18108df004c7b4755b5dd4777f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Aged</topic><topic>Female</topic><topic>Granuloma, Giant Cell - complications</topic><topic>Granuloma, Giant Cell - surgery</topic><topic>hemianopsia</topic><topic>Hemianopsia - etiology</topic><topic>Humans</topic><topic>hypopituitarism</topic><topic>Hypopituitarism - etiology</topic><topic>Hypopituitarism - surgery</topic><topic>Meningitis - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YOSHIOKA, Mitsuaki</creatorcontrib><creatorcontrib>YAMAKAWA, Norio</creatorcontrib><creatorcontrib>SAITO, Hideaki</creatorcontrib><creatorcontrib>YONEDA, Makoto</creatorcontrib><creatorcontrib>NAKAYAMA, Toru</creatorcontrib><creatorcontrib>KUROKI, Mizuo</creatorcontrib><creatorcontrib>TSUCHIDA, Tadashi</creatorcontrib><creatorcontrib>SEKIYA, Masao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YOSHIOKA, Mitsuaki</au><au>YAMAKAWA, Norio</au><au>SAITO, Hideaki</au><au>YONEDA, Makoto</au><au>NAKAYAMA, Toru</au><au>KUROKI, Mizuo</au><au>TSUCHIDA, Tadashi</au><au>SEKIYA, Masao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Granulomatous Hypophysitis with Meningitis and Hypopituitarism</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>1992</date><risdate>1992</risdate><volume>31</volume><issue>9</issue><spage>1147</spage><epage>1150</epage><pages>1147-1150</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>We report an unusual case of granulomatous hypophysitis in which visual impairment, meningitis and hypopituitarism in a 76-year-old female were associated with radiological evidence of a pituitary mass. The sellar lesion was indistinguishable from pituitary tumor on neuroimaging studies, but the recovery of visual acuity and visual field abnormalities together with the improvement of pituitary function after steroid administration indicated that the mass lesion was due to an inflammatory disease of the pituitary gland. The pituitary tissue obtained by transsphenoidal hypophysectomy revealed granulomatous inflammatory cell infiltration with epithelioid cells and scattered multinucleated giant cells. Although a causal relationship with meningitis was not ascertained, possible exposure of the CSF space to the autoimmune inflammatory process of the pituitary gland was likely in view of the positive pituitary antibody reaction and radiological evidence of suprasellar extension. This entity should be considered when evaluating patients with a pituitary mass, hypopituitarism and meningitis. (Internal Medicine 31 : 1147-1150, 1992)</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>1421728</pmid><doi>10.2169/internalmedicine.31.1147</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Female Granuloma, Giant Cell - complications Granuloma, Giant Cell - surgery hemianopsia Hemianopsia - etiology Humans hypopituitarism Hypopituitarism - etiology Hypopituitarism - surgery Meningitis - etiology |
title | Granulomatous Hypophysitis with Meningitis and Hypopituitarism |
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