Two Cases of Segmental Multiple Glomangiomas in a Family: Type 1 or Type 2 Segmental Manifestation?
Several autosomal dominant skin diseases may manifest cutaneous mosaicism. Two types of segmental arrangement can be distinguished: type 1 is characterized by segmental lesions with similar severity to that observed in the diffuse phenotype, the remaining skin being normal; type 2 is characterized b...
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| Veröffentlicht in: | Dermatology (Basel) 2000-01, Vol.201 (1), p.65-67 |
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| creator | Peña-Penabad, C. García-Silva, J. del Pozo, J. Yebra-Pimentel, M.T. Fonseca, E. Cuevas, J. Contreras, F. |
| description | Several autosomal dominant skin diseases may manifest cutaneous mosaicism. Two types of segmental arrangement can be distinguished: type 1 is characterized by segmental lesions with similar severity to that observed in the diffuse phenotype, the remaining skin being normal; type 2 is characterized by segmental lesions showing a major degree of severity and milder lesions diffusely arranged. Multiple glomus tumours have recently been included in the group of genodermatoses showing type 2 segmental involvement. A family with 2 cases of multiple glomangiomas arranged in a segmental fashion is reported. A 12-year-old girl presented multiple nodular glomangiomas on her right buttock and thigh, in a band-like distribution. A sister of her paternal grandfather showed plaque-like multiple glomangiomas on her left thigh and various glomangiomas on her right buttock and arm. No other family members were known to be affected. Two new cases of familial segmental multiple glomangiomas are reported, with the particularity that one of these exhibited type 2 segmental manifestation and the other type 1 from a clinical point of view. |
| doi_str_mv | 10.1159/000018435 |
| format | Article |
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Two types of segmental arrangement can be distinguished: type 1 is characterized by segmental lesions with similar severity to that observed in the diffuse phenotype, the remaining skin being normal; type 2 is characterized by segmental lesions showing a major degree of severity and milder lesions diffusely arranged. Multiple glomus tumours have recently been included in the group of genodermatoses showing type 2 segmental involvement. A family with 2 cases of multiple glomangiomas arranged in a segmental fashion is reported. A 12-year-old girl presented multiple nodular glomangiomas on her right buttock and thigh, in a band-like distribution. A sister of her paternal grandfather showed plaque-like multiple glomangiomas on her left thigh and various glomangiomas on her right buttock and arm. No other family members were known to be affected. Two new cases of familial segmental multiple glomangiomas are reported, with the particularity that one of these exhibited type 2 segmental manifestation and the other type 1 from a clinical point of view.</description><identifier>ISSN: 1018-8665</identifier><identifier>EISSN: 1421-9832</identifier><identifier>DOI: 10.1159/000018435</identifier><identifier>PMID: 10971066</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Biological and medical sciences ; Case Report ; Child ; Dermatology ; Family Health ; Female ; Glomus Tumor - pathology ; Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue ; Humans ; Medical sciences ; Middle Aged ; Neoplasms, Multiple Primary - pathology ; Skin - pathology ; Skin Neoplasms - pathology</subject><ispartof>Dermatology (Basel), 2000-01, Vol.201 (1), p.65-67</ispartof><rights>2000 S. 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Haemangioma of the skin, of mucosae and of soft tissue</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasms, Multiple Primary - pathology</subject><subject>Skin - pathology</subject><subject>Skin Neoplasms - pathology</subject><issn>1018-8665</issn><issn>1421-9832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpt0N1L3TAUAPAwJvNje_BZGEFk4ENd89Gk8UXkzi9QBnr3XE7b5BKXNjVpGfe_X1wvKsM8JIecX84JB6F9kp8QUqjveVqk5Kz4gHYIpyRTJaMfU5xus1KIYhvtxviYFC2l-oS2Sa4kyYXYQc3yj8cLiDpib_CDXnW6H8Hhu8mNdnAaXznfQb-yaY_Y9hjwJXTWrU_xcj1oTLAPc0TfvobeGh1HGK3vzz6jLQMu6i-bcw_9urxYLq6z259XN4vz26xhpRgzroUhus6LttZcABAilBJM1S0zomhlK1leMqUV4Y2SsiSEg6yB0dbwlnHB9tC3ue4Q_NOU2ledjY12Dnrtp1hJShkVXCV4-B989FPo098qKnkaHsufqx3PqAk-xqBNNQTbQVhXJK-ex169jD3Zr5uCU93p9o2c55zA0QZAbMCZAH1j46vjJU00sYOZ_Yaw0uE1v-ly-G72x_3dP1ANrWF_AV0dm4M</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Peña-Penabad, C.</creator><creator>García-Silva, J.</creator><creator>del Pozo, J.</creator><creator>Yebra-Pimentel, M.T.</creator><creator>Fonseca, E.</creator><creator>Cuevas, J.</creator><creator>Contreras, F.</creator><general>Karger</general><general>S. 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Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasms, Multiple Primary - pathology</topic><topic>Skin - pathology</topic><topic>Skin Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peña-Penabad, C.</creatorcontrib><creatorcontrib>García-Silva, J.</creatorcontrib><creatorcontrib>del Pozo, J.</creatorcontrib><creatorcontrib>Yebra-Pimentel, M.T.</creatorcontrib><creatorcontrib>Fonseca, E.</creatorcontrib><creatorcontrib>Cuevas, J.</creatorcontrib><creatorcontrib>Contreras, F.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Dermatology (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peña-Penabad, C.</au><au>García-Silva, J.</au><au>del Pozo, J.</au><au>Yebra-Pimentel, M.T.</au><au>Fonseca, E.</au><au>Cuevas, J.</au><au>Contreras, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two Cases of Segmental Multiple Glomangiomas in a Family: Type 1 or Type 2 Segmental Manifestation?</atitle><jtitle>Dermatology (Basel)</jtitle><addtitle>Dermatology</addtitle><date>2000-01-01</date><risdate>2000</risdate><volume>201</volume><issue>1</issue><spage>65</spage><epage>67</epage><pages>65-67</pages><issn>1018-8665</issn><eissn>1421-9832</eissn><abstract>Several autosomal dominant skin diseases may manifest cutaneous mosaicism. Two types of segmental arrangement can be distinguished: type 1 is characterized by segmental lesions with similar severity to that observed in the diffuse phenotype, the remaining skin being normal; type 2 is characterized by segmental lesions showing a major degree of severity and milder lesions diffusely arranged. Multiple glomus tumours have recently been included in the group of genodermatoses showing type 2 segmental involvement. A family with 2 cases of multiple glomangiomas arranged in a segmental fashion is reported. A 12-year-old girl presented multiple nodular glomangiomas on her right buttock and thigh, in a band-like distribution. A sister of her paternal grandfather showed plaque-like multiple glomangiomas on her left thigh and various glomangiomas on her right buttock and arm. No other family members were known to be affected. Two new cases of familial segmental multiple glomangiomas are reported, with the particularity that one of these exhibited type 2 segmental manifestation and the other type 1 from a clinical point of view.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>10971066</pmid><doi>10.1159/000018435</doi><tpages>3</tpages></addata></record> |
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| ispartof | Dermatology (Basel), 2000-01, Vol.201 (1), p.65-67 |
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| subjects | Biological and medical sciences Case Report Child Dermatology Family Health Female Glomus Tumor - pathology Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue Humans Medical sciences Middle Aged Neoplasms, Multiple Primary - pathology Skin - pathology Skin Neoplasms - pathology |
| title | Two Cases of Segmental Multiple Glomangiomas in a Family: Type 1 or Type 2 Segmental Manifestation? |
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