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Mucormycosis during Imatinib treatment: case report
Philadelphia chromosome positive acute lymphoblastic leukemia is classified as a very high-risk group and it requires an intensive chemotherapy regimen associated with tyrosine-kinase inhibitors and allogeneic hematopoietic stem cell transplant from related or unrelated HLA matched donor. Most times...
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Published in: | Journal of medicine and life 2015-07, Vol.8 (3), p.365-370 |
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creator | Crisan, A M Ghiaur, A Stancioaca, M C Bardas, A Ghita, C Manea, C M Ionescu, B Coriu, D |
description | Philadelphia chromosome positive acute lymphoblastic leukemia is classified as a very high-risk group and it requires an intensive chemotherapy regimen associated with tyrosine-kinase inhibitors and allogeneic hematopoietic stem cell transplant from related or unrelated HLA matched donor. Most times, intensive chemotherapy regimens are associated with prolonged and profound pancytopenia when the risk of invasive fungal infection increases. After Candida and Aspergillus species, Mucormycosis is the third frequent fungal infection in hematology patients and it is associated with a reduced overall survival. When suspected, immediate treatment is needed. We present the case of 24-year-old patient diagnosed with Philadelphia chromosome positive acute lymphoblastic leukemia who developed right rhino-sino-orbital fungal infection with a favorable response to systemic antifungal treatment and noninvasive surgery. Later, patient refused consolidation and allogeneic hematopoietic stem cell transplant from an unrelated HLA matched donor but accepted the first generation tyrosine kinase inhibitor (Imatinib) and maintained a complete hematological and molecular response.
ENT = ear nose throat; BMB = bone marrow biopsy; ALL = acute lymphoblastic leukemia; TKI = tyrosine kinase inhibitor; IFI = invasive fungal infection; BMB = bone marrow biopsy; HE = hematoxylin and eosin; IHC = immunohistochemistry; CD = cluster of differentiation; ob = objective; Tdt = terminal deoxynucleotidyl transferase. |
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ENT = ear nose throat; BMB = bone marrow biopsy; ALL = acute lymphoblastic leukemia; TKI = tyrosine kinase inhibitor; IFI = invasive fungal infection; BMB = bone marrow biopsy; HE = hematoxylin and eosin; IHC = immunohistochemistry; CD = cluster of differentiation; ob = objective; Tdt = terminal deoxynucleotidyl transferase.</description><identifier>ISSN: 1844-122X</identifier><identifier>EISSN: 1844-3117</identifier><identifier>PMID: 26351543</identifier><language>eng</language><publisher>Romania: Carol Daila University Foundation</publisher><subject>Bone Marrow - pathology ; Case Presentations ; Humans ; Imatinib Mesylate - therapeutic use ; Magnetic Resonance Imaging ; Male ; Mucormycosis - complications ; Mucormycosis - drug therapy ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - complications ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy ; Protein Kinase Inhibitors - therapeutic use ; Treatment Outcome ; Young Adult</subject><ispartof>Journal of medicine and life, 2015-07, Vol.8 (3), p.365-370</ispartof><rights>Copyright Carol Davila University Foundation Jul-Sep 2015</rights><rights>Carol Davila University Press 2015</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556922/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556922/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,53782,53784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26351543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Crisan, A M</creatorcontrib><creatorcontrib>Ghiaur, A</creatorcontrib><creatorcontrib>Stancioaca, M C</creatorcontrib><creatorcontrib>Bardas, A</creatorcontrib><creatorcontrib>Ghita, C</creatorcontrib><creatorcontrib>Manea, C M</creatorcontrib><creatorcontrib>Ionescu, B</creatorcontrib><creatorcontrib>Coriu, D</creatorcontrib><title>Mucormycosis during Imatinib treatment: case report</title><title>Journal of medicine and life</title><addtitle>J Med Life</addtitle><description>Philadelphia chromosome positive acute lymphoblastic leukemia is classified as a very high-risk group and it requires an intensive chemotherapy regimen associated with tyrosine-kinase inhibitors and allogeneic hematopoietic stem cell transplant from related or unrelated HLA matched donor. Most times, intensive chemotherapy regimens are associated with prolonged and profound pancytopenia when the risk of invasive fungal infection increases. After Candida and Aspergillus species, Mucormycosis is the third frequent fungal infection in hematology patients and it is associated with a reduced overall survival. When suspected, immediate treatment is needed. We present the case of 24-year-old patient diagnosed with Philadelphia chromosome positive acute lymphoblastic leukemia who developed right rhino-sino-orbital fungal infection with a favorable response to systemic antifungal treatment and noninvasive surgery. Later, patient refused consolidation and allogeneic hematopoietic stem cell transplant from an unrelated HLA matched donor but accepted the first generation tyrosine kinase inhibitor (Imatinib) and maintained a complete hematological and molecular response.
ENT = ear nose throat; BMB = bone marrow biopsy; ALL = acute lymphoblastic leukemia; TKI = tyrosine kinase inhibitor; IFI = invasive fungal infection; BMB = bone marrow biopsy; HE = hematoxylin and eosin; IHC = immunohistochemistry; CD = cluster of differentiation; ob = objective; Tdt = terminal deoxynucleotidyl transferase.</description><subject>Bone Marrow - pathology</subject><subject>Case Presentations</subject><subject>Humans</subject><subject>Imatinib Mesylate - therapeutic use</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Mucormycosis - complications</subject><subject>Mucormycosis - drug therapy</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - complications</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1844-122X</issn><issn>1844-3117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNpdkE1LAzEQhoMoVmr_gix48bKw-dzEgyDFj0LFi4K3ME2zNWV3syZZof_eiFXUucy8zMvLM3OATrBkrKQY14f7GRPyMkGzGLdVLsaFEPQYTYigHHNGTxB9GI0P3c746GKxHoPrN8Wig-R6typSsJA626fLwkC0RbCDD-kUHTXQRjvb9yl6vr15mt-Xy8e7xfx6WQ6kUqkUIIFV1HIqjQVCq6auCGAsayU4Z6qxoJigWRNGpOFYGYyhxisQDbeC0Sm6-sodxlVn1yZzBGj1EFwHYac9OP1307tXvfHvmnEuFCE54GIfEPzbaGPSnYvGti301o9R4xpXSnIi62w9_2fd-jH0-bzsohlZCfJJdPab6Afl-5_0AxUOcgE</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Crisan, A M</creator><creator>Ghiaur, A</creator><creator>Stancioaca, M C</creator><creator>Bardas, A</creator><creator>Ghita, C</creator><creator>Manea, C M</creator><creator>Ionescu, B</creator><creator>Coriu, D</creator><general>Carol Daila University Foundation</general><general>Carol Davila University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BYOGL</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150701</creationdate><title>Mucormycosis during Imatinib treatment: case report</title><author>Crisan, A M ; 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Most times, intensive chemotherapy regimens are associated with prolonged and profound pancytopenia when the risk of invasive fungal infection increases. After Candida and Aspergillus species, Mucormycosis is the third frequent fungal infection in hematology patients and it is associated with a reduced overall survival. When suspected, immediate treatment is needed. We present the case of 24-year-old patient diagnosed with Philadelphia chromosome positive acute lymphoblastic leukemia who developed right rhino-sino-orbital fungal infection with a favorable response to systemic antifungal treatment and noninvasive surgery. Later, patient refused consolidation and allogeneic hematopoietic stem cell transplant from an unrelated HLA matched donor but accepted the first generation tyrosine kinase inhibitor (Imatinib) and maintained a complete hematological and molecular response.
ENT = ear nose throat; BMB = bone marrow biopsy; ALL = acute lymphoblastic leukemia; TKI = tyrosine kinase inhibitor; IFI = invasive fungal infection; BMB = bone marrow biopsy; HE = hematoxylin and eosin; IHC = immunohistochemistry; CD = cluster of differentiation; ob = objective; Tdt = terminal deoxynucleotidyl transferase.</abstract><cop>Romania</cop><pub>Carol Daila University Foundation</pub><pmid>26351543</pmid><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bone Marrow - pathology Case Presentations Humans Imatinib Mesylate - therapeutic use Magnetic Resonance Imaging Male Mucormycosis - complications Mucormycosis - drug therapy Precursor Cell Lymphoblastic Leukemia-Lymphoma - complications Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy Protein Kinase Inhibitors - therapeutic use Treatment Outcome Young Adult |
title | Mucormycosis during Imatinib treatment: case report |
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