Pediatric Parotid Chronic Sclerosing Sialadenitis in an African-American Female: A Rare Case and Review of the Literature

Chronic sclerosing sialadenitis (CSS) or Küttner tumor is an under-recognized, benign fibroinflammatory disease most commonly seen in the submandibular gland of older adult males. Sialolithiasis or bacterial infection was first suspected as an etiology, but CSS is now considered an immunoglobulin G4...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Curēus (Palo Alto, CA) CA), 2020-06, Vol.12 (6)
Hauptverfasser: Keidar, Eytan, Shermetaro, Jacob, Kwartowitz, Gary
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 6
container_start_page
container_title Curēus (Palo Alto, CA)
container_volume 12
creator Keidar, Eytan
Shermetaro, Jacob
Kwartowitz, Gary
description Chronic sclerosing sialadenitis (CSS) or Küttner tumor is an under-recognized, benign fibroinflammatory disease most commonly seen in the submandibular gland of older adult males. Sialolithiasis or bacterial infection was first suspected as an etiology, but CSS is now considered an immunoglobulin G4-related disease (IgG4-RD). IgG4-RD can affect almost every organ in the body, characterized by organ fibrosis with IgG4-positive plasmacytes. Numerous autoimmune-related diseases have been unified under IgG4-RD, including Mikulicz disease (MD), autoimmune pancreatitis, Reidel’s thyroiditis, and others. In any organ, IgG4-RD can present similar to malignancy. Due to the ability to mimic malignancy, it is crucial to be aware of this under-recognized clinical entity. CSS is currently of broad and high clinical interest due to increased understanding, multiorgan involvement, and more clearly defined criteria. To increase awareness of this disease, we describe a rare presentation of CSS with a literature review.
doi_str_mv 10.7759/cureus.8846
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7386075</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2438852731</sourcerecordid><originalsourceid>FETCH-LOGICAL-c283t-3ec45d26f719b9c346ebc386c63a8fd026016a38be8f83658fa696f757234aa23</originalsourceid><addsrcrecordid>eNpVUU1LxDAQDaKoqCf_QMCjVNOkTVIPwrL4BQuKH-cwm07dSDfVJF3x3xtdET3NG-bNm-E9Qg5LdqJU3ZzaMeAYT7Su5AbZ5aXUhS51tfkH75CDGF8YYyVTnCm2TXYEV3UldLNLPu6wdZCCs_QOwpBcS6eLMPjcP9gewxCdf6YPDnpo0bvkInWegqeTLu-ALyZL_Ab0EpfQ4xmd0HsISKcQMfNaeo8rh-906GhaIJ25hAFS_nqfbHXQRzz4qXvk6fLicXpdzG6vbqaTWWG5FqkQaKu65bJTZTNvrKgkzq3Q0koBumsZl6yUIPQcdaeFrHUHssnsWnFRAXCxR87Xuq_jfImtRZ8C9OY1uCWEDzOAM_8n3i3M87AyKl9hqs4CRz8CYXgbMSbzMozB558NzybqmitRZtbxmmWzZzFg93uhZOYrKrOOynxFJT4BiGaHbQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2438852731</pqid></control><display><type>article</type><title>Pediatric Parotid Chronic Sclerosing Sialadenitis in an African-American Female: A Rare Case and Review of the Literature</title><source>PubMed Central Open Access</source><source>PubMed Central</source><creator>Keidar, Eytan ; Shermetaro, Jacob ; Kwartowitz, Gary</creator><creatorcontrib>Keidar, Eytan ; Shermetaro, Jacob ; Kwartowitz, Gary</creatorcontrib><description>Chronic sclerosing sialadenitis (CSS) or Küttner tumor is an under-recognized, benign fibroinflammatory disease most commonly seen in the submandibular gland of older adult males. Sialolithiasis or bacterial infection was first suspected as an etiology, but CSS is now considered an immunoglobulin G4-related disease (IgG4-RD). IgG4-RD can affect almost every organ in the body, characterized by organ fibrosis with IgG4-positive plasmacytes. Numerous autoimmune-related diseases have been unified under IgG4-RD, including Mikulicz disease (MD), autoimmune pancreatitis, Reidel’s thyroiditis, and others. In any organ, IgG4-RD can present similar to malignancy. Due to the ability to mimic malignancy, it is crucial to be aware of this under-recognized clinical entity. CSS is currently of broad and high clinical interest due to increased understanding, multiorgan involvement, and more clearly defined criteria. To increase awareness of this disease, we describe a rare presentation of CSS with a literature review.</description><identifier>ISSN: 2168-8184</identifier><identifier>EISSN: 2168-8184</identifier><identifier>DOI: 10.7759/cureus.8846</identifier><identifier>PMID: 32754389</identifier><language>eng</language><publisher>Palo Alto: Cureus Inc</publisher><subject>African Americans ; Case reports ; Disease ; Epidemiology/Public Health ; Females ; Histology ; Immunoglobulins ; Literature reviews ; Lymphatic system ; Lymphocytes ; Middle age ; Nonsteroidal anti-inflammatory drugs ; Otolaryngology ; Pancreatitis ; Patients ; Pediatrics ; Phlebitis ; Plasma ; Rheumatology ; Ultrasonic imaging</subject><ispartof>Curēus (Palo Alto, CA), 2020-06, Vol.12 (6)</ispartof><rights>Copyright © 2020, Keidar et al. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2020, Keidar et al. 2020 Keidar et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c283t-3ec45d26f719b9c346ebc386c63a8fd026016a38be8f83658fa696f757234aa23</citedby><cites>FETCH-LOGICAL-c283t-3ec45d26f719b9c346ebc386c63a8fd026016a38be8f83658fa696f757234aa23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386075/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386075/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Keidar, Eytan</creatorcontrib><creatorcontrib>Shermetaro, Jacob</creatorcontrib><creatorcontrib>Kwartowitz, Gary</creatorcontrib><title>Pediatric Parotid Chronic Sclerosing Sialadenitis in an African-American Female: A Rare Case and Review of the Literature</title><title>Curēus (Palo Alto, CA)</title><description>Chronic sclerosing sialadenitis (CSS) or Küttner tumor is an under-recognized, benign fibroinflammatory disease most commonly seen in the submandibular gland of older adult males. Sialolithiasis or bacterial infection was first suspected as an etiology, but CSS is now considered an immunoglobulin G4-related disease (IgG4-RD). IgG4-RD can affect almost every organ in the body, characterized by organ fibrosis with IgG4-positive plasmacytes. Numerous autoimmune-related diseases have been unified under IgG4-RD, including Mikulicz disease (MD), autoimmune pancreatitis, Reidel’s thyroiditis, and others. In any organ, IgG4-RD can present similar to malignancy. Due to the ability to mimic malignancy, it is crucial to be aware of this under-recognized clinical entity. CSS is currently of broad and high clinical interest due to increased understanding, multiorgan involvement, and more clearly defined criteria. To increase awareness of this disease, we describe a rare presentation of CSS with a literature review.</description><subject>African Americans</subject><subject>Case reports</subject><subject>Disease</subject><subject>Epidemiology/Public Health</subject><subject>Females</subject><subject>Histology</subject><subject>Immunoglobulins</subject><subject>Literature reviews</subject><subject>Lymphatic system</subject><subject>Lymphocytes</subject><subject>Middle age</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Otolaryngology</subject><subject>Pancreatitis</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Phlebitis</subject><subject>Plasma</subject><subject>Rheumatology</subject><subject>Ultrasonic imaging</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpVUU1LxDAQDaKoqCf_QMCjVNOkTVIPwrL4BQuKH-cwm07dSDfVJF3x3xtdET3NG-bNm-E9Qg5LdqJU3ZzaMeAYT7Su5AbZ5aXUhS51tfkH75CDGF8YYyVTnCm2TXYEV3UldLNLPu6wdZCCs_QOwpBcS6eLMPjcP9gewxCdf6YPDnpo0bvkInWegqeTLu-ALyZL_Ab0EpfQ4xmd0HsISKcQMfNaeo8rh-906GhaIJ25hAFS_nqfbHXQRzz4qXvk6fLicXpdzG6vbqaTWWG5FqkQaKu65bJTZTNvrKgkzq3Q0koBumsZl6yUIPQcdaeFrHUHssnsWnFRAXCxR87Xuq_jfImtRZ8C9OY1uCWEDzOAM_8n3i3M87AyKl9hqs4CRz8CYXgbMSbzMozB558NzybqmitRZtbxmmWzZzFg93uhZOYrKrOOynxFJT4BiGaHbQ</recordid><startdate>20200626</startdate><enddate>20200626</enddate><creator>Keidar, Eytan</creator><creator>Shermetaro, Jacob</creator><creator>Kwartowitz, Gary</creator><general>Cureus Inc</general><general>Cureus</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>5PM</scope></search><sort><creationdate>20200626</creationdate><title>Pediatric Parotid Chronic Sclerosing Sialadenitis in an African-American Female: A Rare Case and Review of the Literature</title><author>Keidar, Eytan ; Shermetaro, Jacob ; Kwartowitz, Gary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c283t-3ec45d26f719b9c346ebc386c63a8fd026016a38be8f83658fa696f757234aa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>African Americans</topic><topic>Case reports</topic><topic>Disease</topic><topic>Epidemiology/Public Health</topic><topic>Females</topic><topic>Histology</topic><topic>Immunoglobulins</topic><topic>Literature reviews</topic><topic>Lymphatic system</topic><topic>Lymphocytes</topic><topic>Middle age</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Otolaryngology</topic><topic>Pancreatitis</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Phlebitis</topic><topic>Plasma</topic><topic>Rheumatology</topic><topic>Ultrasonic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Keidar, Eytan</creatorcontrib><creatorcontrib>Shermetaro, Jacob</creatorcontrib><creatorcontrib>Kwartowitz, Gary</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</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 Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Access via ProQuest (Open Access)</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>PubMed Central (Full Participant titles)</collection><jtitle>Curēus (Palo Alto, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Keidar, Eytan</au><au>Shermetaro, Jacob</au><au>Kwartowitz, Gary</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pediatric Parotid Chronic Sclerosing Sialadenitis in an African-American Female: A Rare Case and Review of the Literature</atitle><jtitle>Curēus (Palo Alto, CA)</jtitle><date>2020-06-26</date><risdate>2020</risdate><volume>12</volume><issue>6</issue><issn>2168-8184</issn><eissn>2168-8184</eissn><abstract>Chronic sclerosing sialadenitis (CSS) or Küttner tumor is an under-recognized, benign fibroinflammatory disease most commonly seen in the submandibular gland of older adult males. Sialolithiasis or bacterial infection was first suspected as an etiology, but CSS is now considered an immunoglobulin G4-related disease (IgG4-RD). IgG4-RD can affect almost every organ in the body, characterized by organ fibrosis with IgG4-positive plasmacytes. Numerous autoimmune-related diseases have been unified under IgG4-RD, including Mikulicz disease (MD), autoimmune pancreatitis, Reidel’s thyroiditis, and others. In any organ, IgG4-RD can present similar to malignancy. Due to the ability to mimic malignancy, it is crucial to be aware of this under-recognized clinical entity. CSS is currently of broad and high clinical interest due to increased understanding, multiorgan involvement, and more clearly defined criteria. To increase awareness of this disease, we describe a rare presentation of CSS with a literature review.</abstract><cop>Palo Alto</cop><pub>Cureus Inc</pub><pmid>32754389</pmid><doi>10.7759/cureus.8846</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2168-8184
ispartof Curēus (Palo Alto, CA), 2020-06, Vol.12 (6)
issn 2168-8184
2168-8184
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7386075
source PubMed Central Open Access; PubMed Central
subjects African Americans
Case reports
Disease
Epidemiology/Public Health
Females
Histology
Immunoglobulins
Literature reviews
Lymphatic system
Lymphocytes
Middle age
Nonsteroidal anti-inflammatory drugs
Otolaryngology
Pancreatitis
Patients
Pediatrics
Phlebitis
Plasma
Rheumatology
Ultrasonic imaging
title Pediatric Parotid Chronic Sclerosing Sialadenitis in an African-American Female: A Rare Case and Review of the Literature
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T17%3A45%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pediatric%20Parotid%20Chronic%20Sclerosing%20Sialadenitis%20in%20an%20African-American%20Female:%20A%20Rare%20Case%20and%20Review%20of%20the%20Literature&rft.jtitle=Cur%C4%93us%20(Palo%20Alto,%20CA)&rft.au=Keidar,%20Eytan&rft.date=2020-06-26&rft.volume=12&rft.issue=6&rft.issn=2168-8184&rft.eissn=2168-8184&rft_id=info:doi/10.7759/cureus.8846&rft_dat=%3Cproquest_pubme%3E2438852731%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2438852731&rft_id=info:pmid/32754389&rfr_iscdi=true