Loading…

A case of ANA-negative systemic sclerosis treated with methylprednisolone

Background: Systemic sclerosis is a multi-systemic disease characterized by excessive fibrosis, inflammation, and vasculopathy. Common clinical features include skin thickening, telangiectasias, salt and pepper skin, beak-shaped nose, and microstomy. We report a case of ANA-negative systemic scleros...

Full description

Saved in:
Bibliographic Details
Published in:Journal of General Procedural Dermatology and Venereology Indonesia 2019-12, Vol.4 (1), p.39-43
Main Authors: Rogacion, Carminda, Uy, Veronica S., Ugalde, Reynaldo L., Vista, Emmerson Gale S.
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 43
container_issue 1
container_start_page 39
container_title Journal of General Procedural Dermatology and Venereology Indonesia
container_volume 4
creator Rogacion, Carminda
Uy, Veronica S.
Ugalde, Reynaldo L.
Vista, Emmerson Gale S.
description Background: Systemic sclerosis is a multi-systemic disease characterized by excessive fibrosis, inflammation, and vasculopathy. Common clinical features include skin thickening, telangiectasias, salt and pepper skin, beak-shaped nose, and microstomy. We report a case of ANA-negative systemic sclerosis in a male patient. Case illustration: Our patient presented with a 10-month history of diffuse hyperpigmentation, skin tightening and decreased mouth aperture, accompanied by digital ulcers, hypopigmented macules and violaceous discoloration of the digits upon exposure to cold temperature. Punch biopsy done revealed mild acanthosis of the epidermis with basal cell layer hyperpigmentation, vacuolar alteration and thickening of the basement membrane zone. ANA was negative. Anti-Scl70 was positive. Patient was treated with methylprednisolone which was tapered over a course of 1 month, with noted decrease in tightening of the skin. Digital ulcers and discoloration of digits upon exposure to cold temperature were no longer observed. Discussion: Diagnosis of systemic sclerosis is made on the presence of scleroderma proximal to the metacarpophalangeal joints, with two of the following minor criteria: sclerodactyly, digital ulcerations or bibasilar pulmonary fibrosis, as well as symptoms involving other organ systems; musculoskeletal, gastrointestinal, respiratory, cardiac, and renal. Conclusion: While the presence of certain distinct features are needed in the diagnosis of systemic sclerosis, a distinct subset of the disease may be ANA-negative and may correspond to better prognosis. A thorough physical and diagnostic examination is needed in order to provide the optimum treatment for each patient. This would prevent systemic complications and further progression of the disease.
doi_str_mv 10.19100/jdvi.v4i1.60
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_22a78412ef284112ab80c0a42b5fa848</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_22a78412ef284112ab80c0a42b5fa848</doaj_id><sourcerecordid>2694410561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1710-8149596f6b3c185e03977056eb54a65e2c0da79af9750321a3cf8f648ced31953</originalsourceid><addsrcrecordid>eNpNkEtrwzAQhE1poSHNsXdDz05XsixLRxP6CIT20p6FLK8SGcdKJScl_75OUkpPMyzD7PAlyT2BOZEE4LFtDm5-YI7MOVwlE8o4ZKWU5Pqfv01mMbYAQIHxEmCSLKvU6Iipt2n1VmU9rvXgDpjGYxxw60waTYfBRxfTIaAesEm_3bBJtzhsjt0uYNO76Dvf411yY3UXcfar0-Tz-elj8Zqt3l-Wi2qVGVISyARhspDc8jo3RBQIuSxLKDjWBdO8QGqg0aXUVpYF5JTo3FhhORMGm5zIIp8my0tv43WrdsFtdTgqr506H3xYKx0GN85WlOpSMELR0lEI1bUAA5rRurBaMDF2PVy6dsF_7TEOqvX70I_zFeWSMTIOI2Mqu6TMCCIGtH9fCagzfHWCr07wFYf8ByMFdpM</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2694410561</pqid></control><display><type>article</type><title>A case of ANA-negative systemic sclerosis treated with methylprednisolone</title><source>Publicly Available Content Database</source><creator>Rogacion, Carminda ; Uy, Veronica S. ; Ugalde, Reynaldo L. ; Vista, Emmerson Gale S.</creator><creatorcontrib>Rogacion, Carminda ; Uy, Veronica S. ; Ugalde, Reynaldo L. ; Vista, Emmerson Gale S.</creatorcontrib><description>Background: Systemic sclerosis is a multi-systemic disease characterized by excessive fibrosis, inflammation, and vasculopathy. Common clinical features include skin thickening, telangiectasias, salt and pepper skin, beak-shaped nose, and microstomy. We report a case of ANA-negative systemic sclerosis in a male patient. Case illustration: Our patient presented with a 10-month history of diffuse hyperpigmentation, skin tightening and decreased mouth aperture, accompanied by digital ulcers, hypopigmented macules and violaceous discoloration of the digits upon exposure to cold temperature. Punch biopsy done revealed mild acanthosis of the epidermis with basal cell layer hyperpigmentation, vacuolar alteration and thickening of the basement membrane zone. ANA was negative. Anti-Scl70 was positive. Patient was treated with methylprednisolone which was tapered over a course of 1 month, with noted decrease in tightening of the skin. Digital ulcers and discoloration of digits upon exposure to cold temperature were no longer observed. Discussion: Diagnosis of systemic sclerosis is made on the presence of scleroderma proximal to the metacarpophalangeal joints, with two of the following minor criteria: sclerodactyly, digital ulcerations or bibasilar pulmonary fibrosis, as well as symptoms involving other organ systems; musculoskeletal, gastrointestinal, respiratory, cardiac, and renal. Conclusion: While the presence of certain distinct features are needed in the diagnosis of systemic sclerosis, a distinct subset of the disease may be ANA-negative and may correspond to better prognosis. A thorough physical and diagnostic examination is needed in order to provide the optimum treatment for each patient. This would prevent systemic complications and further progression of the disease.</description><identifier>ISSN: 2460-7991</identifier><identifier>EISSN: 2460-7991</identifier><identifier>DOI: 10.19100/jdvi.v4i1.60</identifier><language>eng</language><publisher>Depok: Faculty of Medicine Universitas Indonesia</publisher><subject>ana-negative ; diffuse hyperpigmentation ; methylprednisolone ; Scleroderma ; systemic sclerosis ; Ulcers</subject><ispartof>Journal of General Procedural Dermatology and Venereology Indonesia, 2019-12, Vol.4 (1), p.39-43</ispartof><rights>2019. This work is licensed under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2694410561?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,44566</link.rule.ids></links><search><creatorcontrib>Rogacion, Carminda</creatorcontrib><creatorcontrib>Uy, Veronica S.</creatorcontrib><creatorcontrib>Ugalde, Reynaldo L.</creatorcontrib><creatorcontrib>Vista, Emmerson Gale S.</creatorcontrib><title>A case of ANA-negative systemic sclerosis treated with methylprednisolone</title><title>Journal of General Procedural Dermatology and Venereology Indonesia</title><description>Background: Systemic sclerosis is a multi-systemic disease characterized by excessive fibrosis, inflammation, and vasculopathy. Common clinical features include skin thickening, telangiectasias, salt and pepper skin, beak-shaped nose, and microstomy. We report a case of ANA-negative systemic sclerosis in a male patient. Case illustration: Our patient presented with a 10-month history of diffuse hyperpigmentation, skin tightening and decreased mouth aperture, accompanied by digital ulcers, hypopigmented macules and violaceous discoloration of the digits upon exposure to cold temperature. Punch biopsy done revealed mild acanthosis of the epidermis with basal cell layer hyperpigmentation, vacuolar alteration and thickening of the basement membrane zone. ANA was negative. Anti-Scl70 was positive. Patient was treated with methylprednisolone which was tapered over a course of 1 month, with noted decrease in tightening of the skin. Digital ulcers and discoloration of digits upon exposure to cold temperature were no longer observed. Discussion: Diagnosis of systemic sclerosis is made on the presence of scleroderma proximal to the metacarpophalangeal joints, with two of the following minor criteria: sclerodactyly, digital ulcerations or bibasilar pulmonary fibrosis, as well as symptoms involving other organ systems; musculoskeletal, gastrointestinal, respiratory, cardiac, and renal. Conclusion: While the presence of certain distinct features are needed in the diagnosis of systemic sclerosis, a distinct subset of the disease may be ANA-negative and may correspond to better prognosis. A thorough physical and diagnostic examination is needed in order to provide the optimum treatment for each patient. This would prevent systemic complications and further progression of the disease.</description><subject>ana-negative</subject><subject>diffuse hyperpigmentation</subject><subject>methylprednisolone</subject><subject>Scleroderma</subject><subject>systemic sclerosis</subject><subject>Ulcers</subject><issn>2460-7991</issn><issn>2460-7991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNkEtrwzAQhE1poSHNsXdDz05XsixLRxP6CIT20p6FLK8SGcdKJScl_75OUkpPMyzD7PAlyT2BOZEE4LFtDm5-YI7MOVwlE8o4ZKWU5Pqfv01mMbYAQIHxEmCSLKvU6Iipt2n1VmU9rvXgDpjGYxxw60waTYfBRxfTIaAesEm_3bBJtzhsjt0uYNO76Dvf411yY3UXcfar0-Tz-elj8Zqt3l-Wi2qVGVISyARhspDc8jo3RBQIuSxLKDjWBdO8QGqg0aXUVpYF5JTo3FhhORMGm5zIIp8my0tv43WrdsFtdTgqr506H3xYKx0GN85WlOpSMELR0lEI1bUAA5rRurBaMDF2PVy6dsF_7TEOqvX70I_zFeWSMTIOI2Mqu6TMCCIGtH9fCagzfHWCr07wFYf8ByMFdpM</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Rogacion, Carminda</creator><creator>Uy, Veronica S.</creator><creator>Ugalde, Reynaldo L.</creator><creator>Vista, Emmerson Gale S.</creator><general>Faculty of Medicine Universitas Indonesia</general><general>Universitas Indonesia</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20191201</creationdate><title>A case of ANA-negative systemic sclerosis treated with methylprednisolone</title><author>Rogacion, Carminda ; Uy, Veronica S. ; Ugalde, Reynaldo L. ; Vista, Emmerson Gale S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1710-8149596f6b3c185e03977056eb54a65e2c0da79af9750321a3cf8f648ced31953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>ana-negative</topic><topic>diffuse hyperpigmentation</topic><topic>methylprednisolone</topic><topic>Scleroderma</topic><topic>systemic sclerosis</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rogacion, Carminda</creatorcontrib><creatorcontrib>Uy, Veronica S.</creatorcontrib><creatorcontrib>Ugalde, Reynaldo L.</creatorcontrib><creatorcontrib>Vista, Emmerson Gale S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</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>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of General Procedural Dermatology and Venereology Indonesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rogacion, Carminda</au><au>Uy, Veronica S.</au><au>Ugalde, Reynaldo L.</au><au>Vista, Emmerson Gale S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of ANA-negative systemic sclerosis treated with methylprednisolone</atitle><jtitle>Journal of General Procedural Dermatology and Venereology Indonesia</jtitle><date>2019-12-01</date><risdate>2019</risdate><volume>4</volume><issue>1</issue><spage>39</spage><epage>43</epage><pages>39-43</pages><issn>2460-7991</issn><eissn>2460-7991</eissn><abstract>Background: Systemic sclerosis is a multi-systemic disease characterized by excessive fibrosis, inflammation, and vasculopathy. Common clinical features include skin thickening, telangiectasias, salt and pepper skin, beak-shaped nose, and microstomy. We report a case of ANA-negative systemic sclerosis in a male patient. Case illustration: Our patient presented with a 10-month history of diffuse hyperpigmentation, skin tightening and decreased mouth aperture, accompanied by digital ulcers, hypopigmented macules and violaceous discoloration of the digits upon exposure to cold temperature. Punch biopsy done revealed mild acanthosis of the epidermis with basal cell layer hyperpigmentation, vacuolar alteration and thickening of the basement membrane zone. ANA was negative. Anti-Scl70 was positive. Patient was treated with methylprednisolone which was tapered over a course of 1 month, with noted decrease in tightening of the skin. Digital ulcers and discoloration of digits upon exposure to cold temperature were no longer observed. Discussion: Diagnosis of systemic sclerosis is made on the presence of scleroderma proximal to the metacarpophalangeal joints, with two of the following minor criteria: sclerodactyly, digital ulcerations or bibasilar pulmonary fibrosis, as well as symptoms involving other organ systems; musculoskeletal, gastrointestinal, respiratory, cardiac, and renal. Conclusion: While the presence of certain distinct features are needed in the diagnosis of systemic sclerosis, a distinct subset of the disease may be ANA-negative and may correspond to better prognosis. A thorough physical and diagnostic examination is needed in order to provide the optimum treatment for each patient. This would prevent systemic complications and further progression of the disease.</abstract><cop>Depok</cop><pub>Faculty of Medicine Universitas Indonesia</pub><doi>10.19100/jdvi.v4i1.60</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2460-7991
ispartof Journal of General Procedural Dermatology and Venereology Indonesia, 2019-12, Vol.4 (1), p.39-43
issn 2460-7991
2460-7991
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_22a78412ef284112ab80c0a42b5fa848
source Publicly Available Content Database
subjects ana-negative
diffuse hyperpigmentation
methylprednisolone
Scleroderma
systemic sclerosis
Ulcers
title A case of ANA-negative systemic sclerosis treated with methylprednisolone
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T16%3A26%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20case%20of%20ANA-negative%20systemic%20sclerosis%20treated%20with%20methylprednisolone&rft.jtitle=Journal%20of%20General%20Procedural%20Dermatology%20and%20Venereology%20Indonesia&rft.au=Rogacion,%20Carminda&rft.date=2019-12-01&rft.volume=4&rft.issue=1&rft.spage=39&rft.epage=43&rft.pages=39-43&rft.issn=2460-7991&rft.eissn=2460-7991&rft_id=info:doi/10.19100/jdvi.v4i1.60&rft_dat=%3Cproquest_doaj_%3E2694410561%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1710-8149596f6b3c185e03977056eb54a65e2c0da79af9750321a3cf8f648ced31953%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2694410561&rft_id=info:pmid/&rfr_iscdi=true