Loading…
Amyloidosis of submandibular lymph node masquerading as a salivary gland tumor: A rare case report with review of literature
Amyloidosis is a disease characterized by the extracellular deposition of fibrillary proteins causing organ dysfunction. Submandibular lymphadenopathy is a rare clinical presentation of amyloidosis. Majority of the patients progress to develop systemic diseases and usually have AL amyloidosis. Here,...
Saved in:
Published in: | Journal of the scientific society (Belgaum) 2020-09, Vol.47 (3), p.188-191 |
---|---|
Main Authors: | , , , , |
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 | 191 |
container_issue | 3 |
container_start_page | 188 |
container_title | Journal of the scientific society (Belgaum) |
container_volume | 47 |
creator | Mukharji, Snigdha Shruthi, K Date, Amit Sudhamani, S Rao, Rajiv |
description | Amyloidosis is a disease characterized by the extracellular deposition of fibrillary proteins causing organ dysfunction. Submandibular lymphadenopathy is a rare clinical presentation of amyloidosis. Majority of the patients progress to develop systemic diseases and usually have AL amyloidosis. Here, we report a case of a 40-year-old male, who presented with a left submandibular swelling for 3 years. The clinical diagnosis was malignant submandibular salivary gland tumor. Systemic examination was unremarkable. Histopathological examination of the excised swelling revealed effacement of lymph node architecture by an eosinophilic Schiff poor material. Positive Congo red stain with apple-green birefringence on polarization confirmed it as amyloidosis. Serum protein electrophoresis was negative for M Band. Immunohistochemistry revealed kappa light-chain restriction in the deposits, characterizing it as localized primary amyloidosis of the submandibular lymph nodes. |
doi_str_mv | 10.4103/jss.JSS_55_20 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_b84336b0fad64b52a221ab2cfcbe30ab</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A650218559</galeid><doaj_id>oai_doaj_org_article_b84336b0fad64b52a221ab2cfcbe30ab</doaj_id><sourcerecordid>A650218559</sourcerecordid><originalsourceid>FETCH-LOGICAL-c379o-77ef7f7993e53cdd1337e4d7b0c2cc798e34a9fc5793e2f4da9370171d9df1223</originalsourceid><addsrcrecordid>eNptkktr3DAUhU1poUOSZfeCrj3VwxpZ3ZQh9JES6CLtWlzrMdFEsqaSHTPQH1-l06QUIi0kLt85urqcpnlD8LojmL3bl7L-enOjOFcUv2hWlIq-FYSKl80KS9G1HGP5urkoZY_rkoTWwqr5tY3HkLxJxReUHCrzEGE0fpgDZBSO8XCLxmQsilB-zjaD8eMOQUGACgR_D_mIdqEq0DTHlN-jLcqQLdJQLMr2kPKEFj_d1vu9t8vDE8FP1Weasz1vXjkIxV78Pc-aH58-fr_80l5_-3x1ub1uNRMytUJYJ5yQklnOtDGEMWE7IwasqdZC9pZ1IJ3mohLUdQYkE5gIYqRxhFJ21lydfE2CvTpkH2vbKoFXfwop7xTkyetg1dB3jG0G7MBsuoFToJTAQLXTg2UYhur19uR1yKkOpExqn-Y81vYV5YwKTjre_6N2UE396NKUQUdftNpuOKak51xWav0MVbex0es0Wudr_T9BexLonErJ1j19hmD1EANVY6CeYlD5Dyd-SaEOvdyFebFZRWvuxrQ8L1Kk79VjKthvrwi9Fw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2532751458</pqid></control><display><type>article</type><title>Amyloidosis of submandibular lymph node masquerading as a salivary gland tumor: A rare case report with review of literature</title><source>Publicly Available Content Database</source><creator>Mukharji, Snigdha ; Shruthi, K ; Date, Amit ; Sudhamani, S ; Rao, Rajiv</creator><creatorcontrib>Mukharji, Snigdha ; Shruthi, K ; Date, Amit ; Sudhamani, S ; Rao, Rajiv</creatorcontrib><description>Amyloidosis is a disease characterized by the extracellular deposition of fibrillary proteins causing organ dysfunction. Submandibular lymphadenopathy is a rare clinical presentation of amyloidosis. Majority of the patients progress to develop systemic diseases and usually have AL amyloidosis. Here, we report a case of a 40-year-old male, who presented with a left submandibular swelling for 3 years. The clinical diagnosis was malignant submandibular salivary gland tumor. Systemic examination was unremarkable. Histopathological examination of the excised swelling revealed effacement of lymph node architecture by an eosinophilic Schiff poor material. Positive Congo red stain with apple-green birefringence on polarization confirmed it as amyloidosis. Serum protein electrophoresis was negative for M Band. Immunohistochemistry revealed kappa light-chain restriction in the deposits, characterizing it as localized primary amyloidosis of the submandibular lymph nodes.</description><identifier>ISSN: 0974-5009</identifier><identifier>EISSN: 2278-7127</identifier><identifier>DOI: 10.4103/jss.JSS_55_20</identifier><language>eng</language><publisher>Mumbai: Wolters Kluwer India Pvt. Ltd</publisher><subject>amyloidoma ; Amyloidosis ; Birefringence ; Case reports ; Diagnosis ; Electrophoresis ; Immunohistochemistry ; Leukocytes (eosinophilic) ; Literature reviews ; Lymph nodes ; Lymphadenopathy ; Lymphatic system ; Oral cancer ; Proteins ; Salivary gland ; Salivary glands ; Serum proteins ; submandibular swelling ; Swelling ; Tumors</subject><ispartof>Journal of the scientific society (Belgaum), 2020-09, Vol.47 (3), p.188-191</ispartof><rights>COPYRIGHT 2020 Medknow Publications and Media Pvt. Ltd.</rights><rights>2020. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (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/2532751458?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590</link.rule.ids></links><search><creatorcontrib>Mukharji, Snigdha</creatorcontrib><creatorcontrib>Shruthi, K</creatorcontrib><creatorcontrib>Date, Amit</creatorcontrib><creatorcontrib>Sudhamani, S</creatorcontrib><creatorcontrib>Rao, Rajiv</creatorcontrib><title>Amyloidosis of submandibular lymph node masquerading as a salivary gland tumor: A rare case report with review of literature</title><title>Journal of the scientific society (Belgaum)</title><description>Amyloidosis is a disease characterized by the extracellular deposition of fibrillary proteins causing organ dysfunction. Submandibular lymphadenopathy is a rare clinical presentation of amyloidosis. Majority of the patients progress to develop systemic diseases and usually have AL amyloidosis. Here, we report a case of a 40-year-old male, who presented with a left submandibular swelling for 3 years. The clinical diagnosis was malignant submandibular salivary gland tumor. Systemic examination was unremarkable. Histopathological examination of the excised swelling revealed effacement of lymph node architecture by an eosinophilic Schiff poor material. Positive Congo red stain with apple-green birefringence on polarization confirmed it as amyloidosis. Serum protein electrophoresis was negative for M Band. Immunohistochemistry revealed kappa light-chain restriction in the deposits, characterizing it as localized primary amyloidosis of the submandibular lymph nodes.</description><subject>amyloidoma</subject><subject>Amyloidosis</subject><subject>Birefringence</subject><subject>Case reports</subject><subject>Diagnosis</subject><subject>Electrophoresis</subject><subject>Immunohistochemistry</subject><subject>Leukocytes (eosinophilic)</subject><subject>Literature reviews</subject><subject>Lymph nodes</subject><subject>Lymphadenopathy</subject><subject>Lymphatic system</subject><subject>Oral cancer</subject><subject>Proteins</subject><subject>Salivary gland</subject><subject>Salivary glands</subject><subject>Serum proteins</subject><subject>submandibular swelling</subject><subject>Swelling</subject><subject>Tumors</subject><issn>0974-5009</issn><issn>2278-7127</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkktr3DAUhU1poUOSZfeCrj3VwxpZ3ZQh9JES6CLtWlzrMdFEsqaSHTPQH1-l06QUIi0kLt85urqcpnlD8LojmL3bl7L-enOjOFcUv2hWlIq-FYSKl80KS9G1HGP5urkoZY_rkoTWwqr5tY3HkLxJxReUHCrzEGE0fpgDZBSO8XCLxmQsilB-zjaD8eMOQUGACgR_D_mIdqEq0DTHlN-jLcqQLdJQLMr2kPKEFj_d1vu9t8vDE8FP1Weasz1vXjkIxV78Pc-aH58-fr_80l5_-3x1ub1uNRMytUJYJ5yQklnOtDGEMWE7IwasqdZC9pZ1IJ3mohLUdQYkE5gIYqRxhFJ21lydfE2CvTpkH2vbKoFXfwop7xTkyetg1dB3jG0G7MBsuoFToJTAQLXTg2UYhur19uR1yKkOpExqn-Y81vYV5YwKTjre_6N2UE396NKUQUdftNpuOKak51xWav0MVbex0es0Wudr_T9BexLonErJ1j19hmD1EANVY6CeYlD5Dyd-SaEOvdyFebFZRWvuxrQ8L1Kk79VjKthvrwi9Fw</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Mukharji, Snigdha</creator><creator>Shruthi, K</creator><creator>Date, Amit</creator><creator>Sudhamani, S</creator><creator>Rao, Rajiv</creator><general>Wolters Kluwer India Pvt. Ltd</general><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications & Media Pvt. Ltd</general><general>Wolters Kluwer Medknow Publications</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>KB.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M7P</scope><scope>M7S</scope><scope>P5Z</scope><scope>P62</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>DOA</scope></search><sort><creationdate>20200901</creationdate><title>Amyloidosis of submandibular lymph node masquerading as a salivary gland tumor: A rare case report with review of literature</title><author>Mukharji, Snigdha ; Shruthi, K ; Date, Amit ; Sudhamani, S ; Rao, Rajiv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379o-77ef7f7993e53cdd1337e4d7b0c2cc798e34a9fc5793e2f4da9370171d9df1223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>amyloidoma</topic><topic>Amyloidosis</topic><topic>Birefringence</topic><topic>Case reports</topic><topic>Diagnosis</topic><topic>Electrophoresis</topic><topic>Immunohistochemistry</topic><topic>Leukocytes (eosinophilic)</topic><topic>Literature reviews</topic><topic>Lymph nodes</topic><topic>Lymphadenopathy</topic><topic>Lymphatic system</topic><topic>Oral cancer</topic><topic>Proteins</topic><topic>Salivary gland</topic><topic>Salivary glands</topic><topic>Serum proteins</topic><topic>submandibular swelling</topic><topic>Swelling</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukharji, Snigdha</creatorcontrib><creatorcontrib>Shruthi, K</creatorcontrib><creatorcontrib>Date, Amit</creatorcontrib><creatorcontrib>Sudhamani, S</creatorcontrib><creatorcontrib>Rao, Rajiv</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer science database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials science collection</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of the scientific society (Belgaum)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukharji, Snigdha</au><au>Shruthi, K</au><au>Date, Amit</au><au>Sudhamani, S</au><au>Rao, Rajiv</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amyloidosis of submandibular lymph node masquerading as a salivary gland tumor: A rare case report with review of literature</atitle><jtitle>Journal of the scientific society (Belgaum)</jtitle><date>2020-09-01</date><risdate>2020</risdate><volume>47</volume><issue>3</issue><spage>188</spage><epage>191</epage><pages>188-191</pages><issn>0974-5009</issn><eissn>2278-7127</eissn><abstract>Amyloidosis is a disease characterized by the extracellular deposition of fibrillary proteins causing organ dysfunction. Submandibular lymphadenopathy is a rare clinical presentation of amyloidosis. Majority of the patients progress to develop systemic diseases and usually have AL amyloidosis. Here, we report a case of a 40-year-old male, who presented with a left submandibular swelling for 3 years. The clinical diagnosis was malignant submandibular salivary gland tumor. Systemic examination was unremarkable. Histopathological examination of the excised swelling revealed effacement of lymph node architecture by an eosinophilic Schiff poor material. Positive Congo red stain with apple-green birefringence on polarization confirmed it as amyloidosis. Serum protein electrophoresis was negative for M Band. Immunohistochemistry revealed kappa light-chain restriction in the deposits, characterizing it as localized primary amyloidosis of the submandibular lymph nodes.</abstract><cop>Mumbai</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><doi>10.4103/jss.JSS_55_20</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0974-5009 |
ispartof | Journal of the scientific society (Belgaum), 2020-09, Vol.47 (3), p.188-191 |
issn | 0974-5009 2278-7127 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_b84336b0fad64b52a221ab2cfcbe30ab |
source | Publicly Available Content Database |
subjects | amyloidoma Amyloidosis Birefringence Case reports Diagnosis Electrophoresis Immunohistochemistry Leukocytes (eosinophilic) Literature reviews Lymph nodes Lymphadenopathy Lymphatic system Oral cancer Proteins Salivary gland Salivary glands Serum proteins submandibular swelling Swelling Tumors |
title | Amyloidosis of submandibular lymph node masquerading as a salivary gland tumor: A rare case report with review of literature |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T21%3A25%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amyloidosis%20of%20submandibular%20lymph%20node%20masquerading%20as%20a%20salivary%20gland%20tumor:%20A%20rare%20case%20report%20with%20review%20of%20literature&rft.jtitle=Journal%20of%20the%20scientific%20society%20(Belgaum)&rft.au=Mukharji,%20Snigdha&rft.date=2020-09-01&rft.volume=47&rft.issue=3&rft.spage=188&rft.epage=191&rft.pages=188-191&rft.issn=0974-5009&rft.eissn=2278-7127&rft_id=info:doi/10.4103/jss.JSS_55_20&rft_dat=%3Cgale_doaj_%3EA650218559%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c379o-77ef7f7993e53cdd1337e4d7b0c2cc798e34a9fc5793e2f4da9370171d9df1223%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2532751458&rft_id=info:pmid/&rft_galeid=A650218559&rfr_iscdi=true |