Primary spinal extranodal NK/T‐cell lymphoma diagnosed by fine‐needle aspiration and core biopsy
We report an extremely rare case of primary spinal extranodal NK/T‐cell lymphoma (PSENKTL). A 54‐year‐old man presented with fever of unknown etiology for 2 months, with clinical evidence of hemophagocytic lymphohistiocytosis. Imaging studies revealed multiple spinal lesions without evidence of dise...
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Veröffentlicht in: | Diagnostic cytopathology 2023-04, Vol.51 (4), p.E113-E118 |
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description | We report an extremely rare case of primary spinal extranodal NK/T‐cell lymphoma (PSENKTL). A 54‐year‐old man presented with fever of unknown etiology for 2 months, with clinical evidence of hemophagocytic lymphohistiocytosis. Imaging studies revealed multiple spinal lesions without evidence of disease in other body sites. Fine‐needle aspiration and core biopsy (FNACB) of a paraspinal mass showed a monotonous population of intermediate lymphocytes with abundant cytoplasm with fine granules, round to slightly irregular nuclei, and inconspicuous nucleoli. Core biopsy revealed diffuse infiltration by cells with a NK cell phenotype, positive Epstein–Barr virus‐encoded small RNA, and negative T‐cell receptor gene rearrangement. Bone marrow biopsy showed the presence of hemophagocytosis without evidence of lymphoma. The disease disseminated to the small bowel late in the clinical course and the patient died shortly after admission. This unusual case was diagnosed by FNACB and raised awareness of ENKTL as a differential diagnosis in spinal lesions. |
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A 54‐year‐old man presented with fever of unknown etiology for 2 months, with clinical evidence of hemophagocytic lymphohistiocytosis. Imaging studies revealed multiple spinal lesions without evidence of disease in other body sites. Fine‐needle aspiration and core biopsy (FNACB) of a paraspinal mass showed a monotonous population of intermediate lymphocytes with abundant cytoplasm with fine granules, round to slightly irregular nuclei, and inconspicuous nucleoli. Core biopsy revealed diffuse infiltration by cells with a NK cell phenotype, positive Epstein–Barr virus‐encoded small RNA, and negative T‐cell receptor gene rearrangement. Bone marrow biopsy showed the presence of hemophagocytosis without evidence of lymphoma. The disease disseminated to the small bowel late in the clinical course and the patient died shortly after admission. This unusual case was diagnosed by FNACB and raised awareness of ENKTL as a differential diagnosis in spinal lesions.</description><identifier>ISSN: 8755-1039</identifier><identifier>EISSN: 1097-0339</identifier><identifier>DOI: 10.1002/dc.25093</identifier><identifier>PMID: 36585874</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Biopsy ; Biopsy, Fine-Needle ; Biopsy, Large-Core Needle ; EBV‐associated lymphoma ; Epstein-Barr Virus Infections ; extranodal NK/T‐cell lymphoma ; fine needle core biopsy ; fine‐needle aspiration ; Herpesvirus 4, Human ; Humans ; Lymphoma, Extranodal NK-T-Cell - diagnosis ; Lymphoma, Extranodal NK-T-Cell - pathology ; primary spinal lymphoma</subject><ispartof>Diagnostic cytopathology, 2023-04, Vol.51 (4), p.E113-E118</ispartof><rights>2022 Wiley Periodicals LLC.</rights><rights>2023 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3103-7d85a4568a31d3bc9db7105500a134631a8e5665a798d34e733dd70814874e5e3</cites><orcidid>0000-0001-9396-018X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdc.25093$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdc.25093$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36585874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tefft, Jeffrey</creatorcontrib><creatorcontrib>Sheikh‐Fayyaz, Silvat</creatorcontrib><creatorcontrib>Khattar, Pallavi</creatorcontrib><creatorcontrib>Zhang, Xinmin</creatorcontrib><title>Primary spinal extranodal NK/T‐cell lymphoma diagnosed by fine‐needle aspiration and core biopsy</title><title>Diagnostic cytopathology</title><addtitle>Diagn Cytopathol</addtitle><description>We report an extremely rare case of primary spinal extranodal NK/T‐cell lymphoma (PSENKTL). A 54‐year‐old man presented with fever of unknown etiology for 2 months, with clinical evidence of hemophagocytic lymphohistiocytosis. Imaging studies revealed multiple spinal lesions without evidence of disease in other body sites. Fine‐needle aspiration and core biopsy (FNACB) of a paraspinal mass showed a monotonous population of intermediate lymphocytes with abundant cytoplasm with fine granules, round to slightly irregular nuclei, and inconspicuous nucleoli. Core biopsy revealed diffuse infiltration by cells with a NK cell phenotype, positive Epstein–Barr virus‐encoded small RNA, and negative T‐cell receptor gene rearrangement. Bone marrow biopsy showed the presence of hemophagocytosis without evidence of lymphoma. The disease disseminated to the small bowel late in the clinical course and the patient died shortly after admission. This unusual case was diagnosed by FNACB and raised awareness of ENKTL as a differential diagnosis in spinal lesions.</description><subject>Biopsy</subject><subject>Biopsy, Fine-Needle</subject><subject>Biopsy, Large-Core Needle</subject><subject>EBV‐associated lymphoma</subject><subject>Epstein-Barr Virus Infections</subject><subject>extranodal NK/T‐cell lymphoma</subject><subject>fine needle core biopsy</subject><subject>fine‐needle aspiration</subject><subject>Herpesvirus 4, Human</subject><subject>Humans</subject><subject>Lymphoma, Extranodal NK-T-Cell - diagnosis</subject><subject>Lymphoma, Extranodal NK-T-Cell - pathology</subject><subject>primary spinal lymphoma</subject><issn>8755-1039</issn><issn>1097-0339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1u1DAQgC1ExW4XJJ4AWeLCJbvjOP47ouWnqKuWQzlHTjwLWSVxsDeC3HgEnpEnqZe0RULqaebw6dPMR8hLBmsGkG9cvc4FGP6ELBkYlQHn5ilZaiVExoCbBTmP8QAAJmfyGVlwKbTQqlgS9zk0nQ0TjUPT25biz2OwvXdpvbrc3Pz59bvGtqXt1A3ffGepa-zX3kd0tJrovukxET2ia5HapAj22Pie2t7R2gekVeOHOD0nZ3vbRnxxN1fky4f3N9uLbHf98dP27S6reboyU04LWwipLWeOV7VxlWIgBIBlvJCcWY1CSmGV0Y4XqDh3ToFmRXoFBfIVeTN7h-C_jxiPZdfE0_22Rz_GMlfCGKGkgoS-_g89-DGkAidKg5RKqeKfsA4-xoD7cphzlQzKU_nS1eXf8gl9dSccqw7dA3ifOgHZDPxoWpweFZXvtrPwFnRSjEI</recordid><startdate>202304</startdate><enddate>202304</enddate><creator>Tefft, Jeffrey</creator><creator>Sheikh‐Fayyaz, Silvat</creator><creator>Khattar, Pallavi</creator><creator>Zhang, Xinmin</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><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>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9396-018X</orcidid></search><sort><creationdate>202304</creationdate><title>Primary spinal extranodal NK/T‐cell lymphoma diagnosed by fine‐needle aspiration and core biopsy</title><author>Tefft, Jeffrey ; Sheikh‐Fayyaz, Silvat ; Khattar, Pallavi ; Zhang, Xinmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3103-7d85a4568a31d3bc9db7105500a134631a8e5665a798d34e733dd70814874e5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biopsy</topic><topic>Biopsy, Fine-Needle</topic><topic>Biopsy, Large-Core Needle</topic><topic>EBV‐associated lymphoma</topic><topic>Epstein-Barr Virus Infections</topic><topic>extranodal NK/T‐cell lymphoma</topic><topic>fine needle core biopsy</topic><topic>fine‐needle aspiration</topic><topic>Herpesvirus 4, Human</topic><topic>Humans</topic><topic>Lymphoma, Extranodal NK-T-Cell - diagnosis</topic><topic>Lymphoma, Extranodal NK-T-Cell - pathology</topic><topic>primary spinal lymphoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tefft, Jeffrey</creatorcontrib><creatorcontrib>Sheikh‐Fayyaz, Silvat</creatorcontrib><creatorcontrib>Khattar, Pallavi</creatorcontrib><creatorcontrib>Zhang, Xinmin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Diagnostic cytopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tefft, Jeffrey</au><au>Sheikh‐Fayyaz, Silvat</au><au>Khattar, Pallavi</au><au>Zhang, Xinmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary spinal extranodal NK/T‐cell lymphoma diagnosed by fine‐needle aspiration and core biopsy</atitle><jtitle>Diagnostic cytopathology</jtitle><addtitle>Diagn Cytopathol</addtitle><date>2023-04</date><risdate>2023</risdate><volume>51</volume><issue>4</issue><spage>E113</spage><epage>E118</epage><pages>E113-E118</pages><issn>8755-1039</issn><eissn>1097-0339</eissn><abstract>We report an extremely rare case of primary spinal extranodal NK/T‐cell lymphoma (PSENKTL). A 54‐year‐old man presented with fever of unknown etiology for 2 months, with clinical evidence of hemophagocytic lymphohistiocytosis. Imaging studies revealed multiple spinal lesions without evidence of disease in other body sites. Fine‐needle aspiration and core biopsy (FNACB) of a paraspinal mass showed a monotonous population of intermediate lymphocytes with abundant cytoplasm with fine granules, round to slightly irregular nuclei, and inconspicuous nucleoli. Core biopsy revealed diffuse infiltration by cells with a NK cell phenotype, positive Epstein–Barr virus‐encoded small RNA, and negative T‐cell receptor gene rearrangement. Bone marrow biopsy showed the presence of hemophagocytosis without evidence of lymphoma. The disease disseminated to the small bowel late in the clinical course and the patient died shortly after admission. This unusual case was diagnosed by FNACB and raised awareness of ENKTL as a differential diagnosis in spinal lesions.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>36585874</pmid><doi>10.1002/dc.25093</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-9396-018X</orcidid></addata></record> |
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subjects | Biopsy Biopsy, Fine-Needle Biopsy, Large-Core Needle EBV‐associated lymphoma Epstein-Barr Virus Infections extranodal NK/T‐cell lymphoma fine needle core biopsy fine‐needle aspiration Herpesvirus 4, Human Humans Lymphoma, Extranodal NK-T-Cell - diagnosis Lymphoma, Extranodal NK-T-Cell - pathology primary spinal lymphoma |
title | Primary spinal extranodal NK/T‐cell lymphoma diagnosed by fine‐needle aspiration and core biopsy |
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