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Histoid leprosy: clinical and histopathological analysis of patients in follow‐up in University Clinical Hospital of endemic country
Background Histoid leprosy (HL) is a rare form of lepromatous leprosy, characterized by hyperchromic indurated nodules above normal skin. Its main histopathological aspect is spindle cells. Because it may simulate other aspects, such as dermatofibroma and neurofibroma, histoid leprosy poses itself a...
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Published in: | International journal of dermatology 2018-06, Vol.57 (6), p.707-712 |
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container_title | International journal of dermatology |
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creator | Canuto, Maria J. M. Yacoub, Carolina R. D. Trindade, Maria A. B. Avancini, Joao Pagliari, Carla Sotto, Mirian N. |
description | Background
Histoid leprosy (HL) is a rare form of lepromatous leprosy, characterized by hyperchromic indurated nodules above normal skin. Its main histopathological aspect is spindle cells. Because it may simulate other aspects, such as dermatofibroma and neurofibroma, histoid leprosy poses itself as a diagnostic challenge.
Methods
This is a retrospective study with all patients having been selected from the leprosy clinic of the Hospital das Clínicas da Universidade de São Paulo from 2006 to 2016.
Results
There were 12 patients in this study, eight in the histoid group and four in the lepromatous leprosy group. The prevalence of HL was 1.12% in all leprosy subjects. All individuals from HL group were “de novo” cases, and the histopathological analysis of skin lesions presented spindle cells generating a storiform pattern. Immunohistochemistry for CD68, vimentin, and anti‐BCG were positive in all 12 cases. Factor XIIIa was visualized only in the papillary dermis, and S100 protein was negative in all biopsies. Smooth‐muscle actin was present in 62.5% of the HL samples.
Conclusion
The prevalence of HL was similar to previous reports. However, all histoid patients were “de novo” cases, differing from published studies. Fusocellular macrophage transformation could be explained by the differences in cytoskeleton proteins expressed in histoid lesions in comparison to other leprosy variants, with emphasis on vimentin and smooth muscle actin. |
doi_str_mv | 10.1111/ijd.13926 |
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Histoid leprosy (HL) is a rare form of lepromatous leprosy, characterized by hyperchromic indurated nodules above normal skin. Its main histopathological aspect is spindle cells. Because it may simulate other aspects, such as dermatofibroma and neurofibroma, histoid leprosy poses itself as a diagnostic challenge.
Methods
This is a retrospective study with all patients having been selected from the leprosy clinic of the Hospital das Clínicas da Universidade de São Paulo from 2006 to 2016.
Results
There were 12 patients in this study, eight in the histoid group and four in the lepromatous leprosy group. The prevalence of HL was 1.12% in all leprosy subjects. All individuals from HL group were “de novo” cases, and the histopathological analysis of skin lesions presented spindle cells generating a storiform pattern. Immunohistochemistry for CD68, vimentin, and anti‐BCG were positive in all 12 cases. Factor XIIIa was visualized only in the papillary dermis, and S100 protein was negative in all biopsies. Smooth‐muscle actin was present in 62.5% of the HL samples.
Conclusion
The prevalence of HL was similar to previous reports. However, all histoid patients were “de novo” cases, differing from published studies. Fusocellular macrophage transformation could be explained by the differences in cytoskeleton proteins expressed in histoid lesions in comparison to other leprosy variants, with emphasis on vimentin and smooth muscle actin.</description><identifier>ISSN: 0011-9059</identifier><identifier>EISSN: 1365-4632</identifier><identifier>DOI: 10.1111/ijd.13926</identifier><identifier>PMID: 29384191</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Actin ; Bacillus Calmette-Guerin vaccine ; BCG ; Cytoskeleton ; Dermis ; Diagnostic systems ; Genetic transformation ; Immunohistochemistry ; Leprosy ; Lesions ; Macrophages ; Muscles ; Nodules ; Patients ; Proteins ; S100 protein ; Skin diseases ; Smooth muscle ; Vimentin</subject><ispartof>International journal of dermatology, 2018-06, Vol.57 (6), p.707-712</ispartof><rights>2018</rights><rights>2018 The International Society of Dermatology.</rights><rights>International Journal of Dermatology © 2018 International Society of Dermatology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-7ac3fbe75b34c17fb9d06b6c22ce2d9412bd9c7ae7640f6e4e1421c45233a5c23</citedby><cites>FETCH-LOGICAL-c3536-7ac3fbe75b34c17fb9d06b6c22ce2d9412bd9c7ae7640f6e4e1421c45233a5c23</cites><orcidid>0000-0003-3038-6373</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29384191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Canuto, Maria J. M.</creatorcontrib><creatorcontrib>Yacoub, Carolina R. D.</creatorcontrib><creatorcontrib>Trindade, Maria A. B.</creatorcontrib><creatorcontrib>Avancini, Joao</creatorcontrib><creatorcontrib>Pagliari, Carla</creatorcontrib><creatorcontrib>Sotto, Mirian N.</creatorcontrib><title>Histoid leprosy: clinical and histopathological analysis of patients in follow‐up in University Clinical Hospital of endemic country</title><title>International journal of dermatology</title><addtitle>Int J Dermatol</addtitle><description>Background
Histoid leprosy (HL) is a rare form of lepromatous leprosy, characterized by hyperchromic indurated nodules above normal skin. Its main histopathological aspect is spindle cells. Because it may simulate other aspects, such as dermatofibroma and neurofibroma, histoid leprosy poses itself as a diagnostic challenge.
Methods
This is a retrospective study with all patients having been selected from the leprosy clinic of the Hospital das Clínicas da Universidade de São Paulo from 2006 to 2016.
Results
There were 12 patients in this study, eight in the histoid group and four in the lepromatous leprosy group. The prevalence of HL was 1.12% in all leprosy subjects. All individuals from HL group were “de novo” cases, and the histopathological analysis of skin lesions presented spindle cells generating a storiform pattern. Immunohistochemistry for CD68, vimentin, and anti‐BCG were positive in all 12 cases. Factor XIIIa was visualized only in the papillary dermis, and S100 protein was negative in all biopsies. Smooth‐muscle actin was present in 62.5% of the HL samples.
Conclusion
The prevalence of HL was similar to previous reports. However, all histoid patients were “de novo” cases, differing from published studies. Fusocellular macrophage transformation could be explained by the differences in cytoskeleton proteins expressed in histoid lesions in comparison to other leprosy variants, with emphasis on vimentin and smooth muscle actin.</description><subject>Actin</subject><subject>Bacillus Calmette-Guerin vaccine</subject><subject>BCG</subject><subject>Cytoskeleton</subject><subject>Dermis</subject><subject>Diagnostic systems</subject><subject>Genetic transformation</subject><subject>Immunohistochemistry</subject><subject>Leprosy</subject><subject>Lesions</subject><subject>Macrophages</subject><subject>Muscles</subject><subject>Nodules</subject><subject>Patients</subject><subject>Proteins</subject><subject>S100 protein</subject><subject>Skin diseases</subject><subject>Smooth muscle</subject><subject>Vimentin</subject><issn>0011-9059</issn><issn>1365-4632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kT1v2zAQhomiQe18DP0DBYEuyaCEX6LKboWT1gkMZElmgqJONQ1aVESpgbZMmfMb-0tKx3aGArmFd7znXuDuRegzJec0xYVbVeeUKyY_oCnlMs-E5OwjmhJCaaZIriboMMZVKjmj4hOaMMW_CaroFD3PXeyDq7CHtgtx_I6td42zxmPTVHi56bamXwYffu9-jR-jizjUODUcNH3ErsF18D48_n16GdpNed-4P9BF1494thech9i6PiVpFJoK1s5iG4am78ZjdFAbH-Fk9x6h-59Xd7N5trj9dT37scgsz7nMCmN5XUKRl1xYWtSlqogspWXMAquUoKyslC0MFFKQWoIAKhi1Imecm9wyfoROt7pp2YcBYq_XLlrw3jQQhqipUjwdTRYyoV__Q1dh6NL2UTPCJedEUpKosy1l0_ViB7VuO7c23agp0RtzdDJHv5qT2C87xaFcQ_VG7t1IwMUWeHQexveV9PXN5VbyHydrm7A</recordid><startdate>201806</startdate><enddate>201806</enddate><creator>Canuto, Maria J. M.</creator><creator>Yacoub, Carolina R. D.</creator><creator>Trindade, Maria A. B.</creator><creator>Avancini, Joao</creator><creator>Pagliari, Carla</creator><creator>Sotto, Mirian N.</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3038-6373</orcidid></search><sort><creationdate>201806</creationdate><title>Histoid leprosy: clinical and histopathological analysis of patients in follow‐up in University Clinical Hospital of endemic country</title><author>Canuto, Maria J. M. ; Yacoub, Carolina R. D. ; Trindade, Maria A. B. ; Avancini, Joao ; Pagliari, Carla ; Sotto, Mirian N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-7ac3fbe75b34c17fb9d06b6c22ce2d9412bd9c7ae7640f6e4e1421c45233a5c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Actin</topic><topic>Bacillus Calmette-Guerin vaccine</topic><topic>BCG</topic><topic>Cytoskeleton</topic><topic>Dermis</topic><topic>Diagnostic systems</topic><topic>Genetic transformation</topic><topic>Immunohistochemistry</topic><topic>Leprosy</topic><topic>Lesions</topic><topic>Macrophages</topic><topic>Muscles</topic><topic>Nodules</topic><topic>Patients</topic><topic>Proteins</topic><topic>S100 protein</topic><topic>Skin diseases</topic><topic>Smooth muscle</topic><topic>Vimentin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Canuto, Maria J. M.</creatorcontrib><creatorcontrib>Yacoub, Carolina R. D.</creatorcontrib><creatorcontrib>Trindade, Maria A. B.</creatorcontrib><creatorcontrib>Avancini, Joao</creatorcontrib><creatorcontrib>Pagliari, Carla</creatorcontrib><creatorcontrib>Sotto, Mirian N.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Canuto, Maria J. M.</au><au>Yacoub, Carolina R. D.</au><au>Trindade, Maria A. B.</au><au>Avancini, Joao</au><au>Pagliari, Carla</au><au>Sotto, Mirian N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histoid leprosy: clinical and histopathological analysis of patients in follow‐up in University Clinical Hospital of endemic country</atitle><jtitle>International journal of dermatology</jtitle><addtitle>Int J Dermatol</addtitle><date>2018-06</date><risdate>2018</risdate><volume>57</volume><issue>6</issue><spage>707</spage><epage>712</epage><pages>707-712</pages><issn>0011-9059</issn><eissn>1365-4632</eissn><abstract>Background
Histoid leprosy (HL) is a rare form of lepromatous leprosy, characterized by hyperchromic indurated nodules above normal skin. Its main histopathological aspect is spindle cells. Because it may simulate other aspects, such as dermatofibroma and neurofibroma, histoid leprosy poses itself as a diagnostic challenge.
Methods
This is a retrospective study with all patients having been selected from the leprosy clinic of the Hospital das Clínicas da Universidade de São Paulo from 2006 to 2016.
Results
There were 12 patients in this study, eight in the histoid group and four in the lepromatous leprosy group. The prevalence of HL was 1.12% in all leprosy subjects. All individuals from HL group were “de novo” cases, and the histopathological analysis of skin lesions presented spindle cells generating a storiform pattern. Immunohistochemistry for CD68, vimentin, and anti‐BCG were positive in all 12 cases. Factor XIIIa was visualized only in the papillary dermis, and S100 protein was negative in all biopsies. Smooth‐muscle actin was present in 62.5% of the HL samples.
Conclusion
The prevalence of HL was similar to previous reports. However, all histoid patients were “de novo” cases, differing from published studies. Fusocellular macrophage transformation could be explained by the differences in cytoskeleton proteins expressed in histoid lesions in comparison to other leprosy variants, with emphasis on vimentin and smooth muscle actin.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>29384191</pmid><doi>10.1111/ijd.13926</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3038-6373</orcidid></addata></record> |
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subjects | Actin Bacillus Calmette-Guerin vaccine BCG Cytoskeleton Dermis Diagnostic systems Genetic transformation Immunohistochemistry Leprosy Lesions Macrophages Muscles Nodules Patients Proteins S100 protein Skin diseases Smooth muscle Vimentin |
title | Histoid leprosy: clinical and histopathological analysis of patients in follow‐up in University Clinical Hospital of endemic country |
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