Psammomatous melanotic schwannoma of a spinal nerve root. Relationship with the Carney complex
A 36-year-old man had an oval, black, extradural tumor partly removed from the left C4 spinal root, with total removal 4 months later. In both specimens, most tumor cells were spindle-shaped. A few cells were large, epithelioid-like, with a prominent nucleolus. Mitoses were rarely seen. Many tumor c...
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Veröffentlicht in: | Pathology, research and practice research and practice, 1996-11, Vol.192 (11), p.1142-6; discussion 1147 |
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creator | Léger, F Vital, C Rivel, J Benjelloun, B San Galli, F Guérin, J |
description | A 36-year-old man had an oval, black, extradural tumor partly removed from the left C4 spinal root, with total removal 4 months later. In both specimens, most tumor cells were spindle-shaped. A few cells were large, epithelioid-like, with a prominent nucleolus. Mitoses were rarely seen. Many tumor cells contained coarse or fine granules of a brown pigment. Such cells were immunopositive for S-100 protein and HMB-45. Additionally, psammoma bodies were numerous in certain areas, indicating a diagnosis of psammomatous melanotic schwannoma (PMS). Periumbilical spotty pigmentation was found in the patient and in six of his siblings and their mother. The search for cardiac myxoma and endocrine overactivity was negative in the patient. Features of Carney's complex must be sought in a patient with PMS and in their primary relatives. So far, more than 150 patients and seven families with Carney's complex have been reported. |
doi_str_mv | 10.1016/S0344-0338(96)80034-3 |
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Relationship with the Carney complex</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Léger, F ; Vital, C ; Rivel, J ; Benjelloun, B ; San Galli, F ; Guérin, J</creator><creatorcontrib>Léger, F ; Vital, C ; Rivel, J ; Benjelloun, B ; San Galli, F ; Guérin, J</creatorcontrib><description>A 36-year-old man had an oval, black, extradural tumor partly removed from the left C4 spinal root, with total removal 4 months later. In both specimens, most tumor cells were spindle-shaped. A few cells were large, epithelioid-like, with a prominent nucleolus. Mitoses were rarely seen. Many tumor cells contained coarse or fine granules of a brown pigment. Such cells were immunopositive for S-100 protein and HMB-45. Additionally, psammoma bodies were numerous in certain areas, indicating a diagnosis of psammomatous melanotic schwannoma (PMS). Periumbilical spotty pigmentation was found in the patient and in six of his siblings and their mother. The search for cardiac myxoma and endocrine overactivity was negative in the patient. Features of Carney's complex must be sought in a patient with PMS and in their primary relatives. So far, more than 150 patients and seven families with Carney's complex have been reported.</description><identifier>ISSN: 0344-0338</identifier><identifier>DOI: 10.1016/S0344-0338(96)80034-3</identifier><identifier>PMID: 9122034</identifier><language>eng</language><publisher>Germany</publisher><subject>Adult ; Humans ; Immunohistochemistry ; Male ; Microscopy, Electron ; Neurilemmoma - complications ; Neurilemmoma - metabolism ; Neurilemmoma - pathology ; Peripheral Nervous System Neoplasms - complications ; Peripheral Nervous System Neoplasms - metabolism ; Peripheral Nervous System Neoplasms - pathology ; Pigmentation Disorders - complications ; Pigmentation Disorders - genetics ; Pigmentation Disorders - pathology ; Spinal Nerve Roots ; Syndrome</subject><ispartof>Pathology, research and practice, 1996-11, Vol.192 (11), p.1142-6; discussion 1147</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9122034$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Léger, F</creatorcontrib><creatorcontrib>Vital, C</creatorcontrib><creatorcontrib>Rivel, J</creatorcontrib><creatorcontrib>Benjelloun, B</creatorcontrib><creatorcontrib>San Galli, F</creatorcontrib><creatorcontrib>Guérin, J</creatorcontrib><title>Psammomatous melanotic schwannoma of a spinal nerve root. Relationship with the Carney complex</title><title>Pathology, research and practice</title><addtitle>Pathol Res Pract</addtitle><description>A 36-year-old man had an oval, black, extradural tumor partly removed from the left C4 spinal root, with total removal 4 months later. In both specimens, most tumor cells were spindle-shaped. A few cells were large, epithelioid-like, with a prominent nucleolus. Mitoses were rarely seen. Many tumor cells contained coarse or fine granules of a brown pigment. Such cells were immunopositive for S-100 protein and HMB-45. Additionally, psammoma bodies were numerous in certain areas, indicating a diagnosis of psammomatous melanotic schwannoma (PMS). Periumbilical spotty pigmentation was found in the patient and in six of his siblings and their mother. The search for cardiac myxoma and endocrine overactivity was negative in the patient. Features of Carney's complex must be sought in a patient with PMS and in their primary relatives. So far, more than 150 patients and seven families with Carney's complex have been reported.</description><subject>Adult</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Microscopy, Electron</subject><subject>Neurilemmoma - complications</subject><subject>Neurilemmoma - metabolism</subject><subject>Neurilemmoma - pathology</subject><subject>Peripheral Nervous System Neoplasms - complications</subject><subject>Peripheral Nervous System Neoplasms - metabolism</subject><subject>Peripheral Nervous System Neoplasms - pathology</subject><subject>Pigmentation Disorders - complications</subject><subject>Pigmentation Disorders - genetics</subject><subject>Pigmentation Disorders - pathology</subject><subject>Spinal Nerve Roots</subject><subject>Syndrome</subject><issn>0344-0338</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtLAzEUhbNQaq3-hEJWoovRvEwySym-oKD42DpkMgkTmSTjJLX23xuwuDrccz4unAPAEqNLjDC_ekWUsQpRKs9rfiFROSt6AOb_9hE4TukTISQQwzMwqzEhJZyDj-ekvI9e5bhJ0JtBhZidhkn3WxVCCWC0UME0uqAGGMz0beAUY76ELwXOLobUuxFuXe5h7g1cqSmYHdTRj4P5OQGHVg3JnO51Ad7vbt9WD9X66f5xdbOuRoJ4roS2LeISt52RtkZK1YzrDltLTSeI7AiVvBVctIoRTAXnrNOsVahmGhtLLF2As7-_4xS_NiblxrukzVDqmFKsEZJLia95AZd7cNN60zXj5Lyads1-EPoLDktjFw</recordid><startdate>19961101</startdate><enddate>19961101</enddate><creator>Léger, F</creator><creator>Vital, C</creator><creator>Rivel, J</creator><creator>Benjelloun, B</creator><creator>San Galli, F</creator><creator>Guérin, J</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19961101</creationdate><title>Psammomatous melanotic schwannoma of a spinal nerve root. 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Relationship with the Carney complex</atitle><jtitle>Pathology, research and practice</jtitle><addtitle>Pathol Res Pract</addtitle><date>1996-11-01</date><risdate>1996</risdate><volume>192</volume><issue>11</issue><spage>1142</spage><epage>6; discussion 1147</epage><pages>1142-6; discussion 1147</pages><issn>0344-0338</issn><abstract>A 36-year-old man had an oval, black, extradural tumor partly removed from the left C4 spinal root, with total removal 4 months later. In both specimens, most tumor cells were spindle-shaped. A few cells were large, epithelioid-like, with a prominent nucleolus. Mitoses were rarely seen. Many tumor cells contained coarse or fine granules of a brown pigment. Such cells were immunopositive for S-100 protein and HMB-45. Additionally, psammoma bodies were numerous in certain areas, indicating a diagnosis of psammomatous melanotic schwannoma (PMS). Periumbilical spotty pigmentation was found in the patient and in six of his siblings and their mother. The search for cardiac myxoma and endocrine overactivity was negative in the patient. Features of Carney's complex must be sought in a patient with PMS and in their primary relatives. So far, more than 150 patients and seven families with Carney's complex have been reported.</abstract><cop>Germany</cop><pmid>9122034</pmid><doi>10.1016/S0344-0338(96)80034-3</doi></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Adult Humans Immunohistochemistry Male Microscopy, Electron Neurilemmoma - complications Neurilemmoma - metabolism Neurilemmoma - pathology Peripheral Nervous System Neoplasms - complications Peripheral Nervous System Neoplasms - metabolism Peripheral Nervous System Neoplasms - pathology Pigmentation Disorders - complications Pigmentation Disorders - genetics Pigmentation Disorders - pathology Spinal Nerve Roots Syndrome |
title | Psammomatous melanotic schwannoma of a spinal nerve root. Relationship with the Carney complex |
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