Chronologic aging in black skin
Histologic studies examining chronologic aging in skin have been confined to white skin. In the present study, we examined the features of sun-protected black skin from individuals 6 weeks to 75 years of age with light and electron microscopy. With age, the dermoepidermal junction became flattened w...
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Veröffentlicht in: | The American journal of dermatopathology 1989-08, Vol.11 (4), p.319-328 |
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description | Histologic studies examining chronologic aging in skin have been confined to white skin. In the present study, we examined the features of sun-protected black skin from individuals 6 weeks to 75 years of age with light and electron microscopy. With age, the dermoepidermal junction became flattened with multiple zones of basal lamina and anchoring fibril reduplication. Microfibrils in the papillary dermis became somewhat more irregularly oriented. Compact elastic fibers showed cystic changes and separation of skeleton fibers with age. The area occupied by the superficial vascular plexus in specimens of equal epidermal surface length decreased from the infant to young adult (21-29 years old) to adult (39-52 years old) age groups, then increased in the aged adult (73-75 years old) age group. With the exception of the vascularity in the aged adult group, the above features are similar to those seen in aging white skin, and suggest that chronologic aging in white and black skin is similar. In addition, there was a decrease in the number of melanocytes with age. Basal keratinocyte melanin granule density increased with age to age 52 and remained dense in the aged adult group, even as the number of melanocytes decreased. |
doi_str_mv | 10.1097/00000372-198908000-00005 |
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With the exception of the vascularity in the aged adult group, the above features are similar to those seen in aging white skin, and suggest that chronologic aging in white and black skin is similar. In addition, there was a decrease in the number of melanocytes with age. Basal keratinocyte melanin granule density increased with age to age 52 and remained dense in the aged adult group, even as the number of melanocytes decreased.</description><identifier>ISSN: 0193-1091</identifier><identifier>EISSN: 1533-0311</identifier><identifier>DOI: 10.1097/00000372-198908000-00005</identifier><identifier>PMID: 2774101</identifier><identifier>CODEN: AJODDB</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; African Continental Ancestry Group ; Aging - pathology ; Biological and medical sciences ; Epidermis - pathology ; Epidermis - ultrastructure ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Infant ; Male ; Melanocytes - pathology ; Melanocytes - ultrastructure ; Microscopy, Electron ; Middle Aged ; Skin - pathology ; Skin - ultrastructure ; Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue</subject><ispartof>The American journal of dermatopathology, 1989-08, Vol.11 (4), p.319-328</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-94bb8dde626bcab8c1113df9beaed4a066f4ef69020d96e35aa8f21ee1ff01ba3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19275697$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2774101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HERZBERG, A. J</creatorcontrib><creatorcontrib>DINEHART, S. M</creatorcontrib><title>Chronologic aging in black skin</title><title>The American journal of dermatopathology</title><addtitle>Am J Dermatopathol</addtitle><description>Histologic studies examining chronologic aging in skin have been confined to white skin. In the present study, we examined the features of sun-protected black skin from individuals 6 weeks to 75 years of age with light and electron microscopy. With age, the dermoepidermal junction became flattened with multiple zones of basal lamina and anchoring fibril reduplication. Microfibrils in the papillary dermis became somewhat more irregularly oriented. Compact elastic fibers showed cystic changes and separation of skeleton fibers with age. The area occupied by the superficial vascular plexus in specimens of equal epidermal surface length decreased from the infant to young adult (21-29 years old) to adult (39-52 years old) age groups, then increased in the aged adult (73-75 years old) age group. With the exception of the vascularity in the aged adult group, the above features are similar to those seen in aging white skin, and suggest that chronologic aging in white and black skin is similar. In addition, there was a decrease in the number of melanocytes with age. Basal keratinocyte melanin granule density increased with age to age 52 and remained dense in the aged adult group, even as the number of melanocytes decreased.</description><subject>Adult</subject><subject>African Continental Ancestry Group</subject><subject>Aging - pathology</subject><subject>Biological and medical sciences</subject><subject>Epidermis - pathology</subject><subject>Epidermis - ultrastructure</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Melanocytes - pathology</subject><subject>Melanocytes - ultrastructure</subject><subject>Microscopy, Electron</subject><subject>Middle Aged</subject><subject>Skin - pathology</subject><subject>Skin - ultrastructure</subject><subject>Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue</subject><issn>0193-1091</issn><issn>1533-0311</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUDtPwzAQthColMJPQGSBLXBnJ048ooqXVIkF5ujs2MU0TYrdDPx7UhrKLaf7Xid9jCUItwiquIPdiIKnqEoF5XCkOyQ_YlPMhUhBIB6zKaAS6WDAU3YW4ycA8hLyCZvwosgQcMqu5h-ha7umW3qT0NK3y8S3iW7IrJK48u05O3HURHsx7hl7f3x4mz-ni9enl_n9IjUig22qMq3LuraSS21IlwYRRe2UtmTrjEBKl1knFXColbQiJyodR2vROUBNYsZu9rmb0H31Nm6rtY_GNg21tutjVSgOIHk2CMu90IQuxmBdtQl-TeG7Qqh23VR_3VSHbn6hfLBejj96vbb1wTiWMfDXI0_RUOMCtcbH_3zFi1yqQvwAwkpq2g</recordid><startdate>19890801</startdate><enddate>19890801</enddate><creator>HERZBERG, A. J</creator><creator>DINEHART, S. M</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><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>19890801</creationdate><title>Chronologic aging in black skin</title><author>HERZBERG, A. J ; DINEHART, S. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-94bb8dde626bcab8c1113df9beaed4a066f4ef69020d96e35aa8f21ee1ff01ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adult</topic><topic>African Continental Ancestry Group</topic><topic>Aging - pathology</topic><topic>Biological and medical sciences</topic><topic>Epidermis - pathology</topic><topic>Epidermis - ultrastructure</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Melanocytes - pathology</topic><topic>Melanocytes - ultrastructure</topic><topic>Microscopy, Electron</topic><topic>Middle Aged</topic><topic>Skin - pathology</topic><topic>Skin - ultrastructure</topic><topic>Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HERZBERG, A. J</creatorcontrib><creatorcontrib>DINEHART, S. 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M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronologic aging in black skin</atitle><jtitle>The American journal of dermatopathology</jtitle><addtitle>Am J Dermatopathol</addtitle><date>1989-08-01</date><risdate>1989</risdate><volume>11</volume><issue>4</issue><spage>319</spage><epage>328</epage><pages>319-328</pages><issn>0193-1091</issn><eissn>1533-0311</eissn><coden>AJODDB</coden><abstract>Histologic studies examining chronologic aging in skin have been confined to white skin. In the present study, we examined the features of sun-protected black skin from individuals 6 weeks to 75 years of age with light and electron microscopy. With age, the dermoepidermal junction became flattened with multiple zones of basal lamina and anchoring fibril reduplication. Microfibrils in the papillary dermis became somewhat more irregularly oriented. Compact elastic fibers showed cystic changes and separation of skeleton fibers with age. The area occupied by the superficial vascular plexus in specimens of equal epidermal surface length decreased from the infant to young adult (21-29 years old) to adult (39-52 years old) age groups, then increased in the aged adult (73-75 years old) age group. With the exception of the vascularity in the aged adult group, the above features are similar to those seen in aging white skin, and suggest that chronologic aging in white and black skin is similar. In addition, there was a decrease in the number of melanocytes with age. Basal keratinocyte melanin granule density increased with age to age 52 and remained dense in the aged adult group, even as the number of melanocytes decreased.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>2774101</pmid><doi>10.1097/00000372-198908000-00005</doi><tpages>10</tpages></addata></record> |
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subjects | Adult African Continental Ancestry Group Aging - pathology Biological and medical sciences Epidermis - pathology Epidermis - ultrastructure Female Fundamental and applied biological sciences. Psychology Humans Infant Male Melanocytes - pathology Melanocytes - ultrastructure Microscopy, Electron Middle Aged Skin - pathology Skin - ultrastructure Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue |
title | Chronologic aging in black skin |
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