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Multiple diagnostic methods for mucormycosis: A retrospective case series
Background Mucormycosis is a rare invasive fungal disease with high mortality. Early diagnosis and targeted drugs are crucial to improving clinical outcomes. Methods We searched the electronic hospital database of the First Affiliated Hospital of Zhejiang University School of Medicine for adult pati...
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Published in: | Journal of clinical laboratory analysis 2022-08, Vol.36 (8), p.e24588-n/a |
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description | Background
Mucormycosis is a rare invasive fungal disease with high mortality. Early diagnosis and targeted drugs are crucial to improving clinical outcomes.
Methods
We searched the electronic hospital database of the First Affiliated Hospital of Zhejiang University School of Medicine for adult patients with mucormycosis between 2000 and 2021. Demographic, clinical, treatment, and outcome data were collected and compared with the data in the relevant literature.
Results
Eleven cases of mucormycosis—four of multisite infection, one of skin infection, five of lung infection, and one of gastrointestinal infection—were found and analyzed. The patients were diagnosed mainly based on pathological and histological findings, and three patients had metagenomic next‐generation sequencing findings. Delayed diagnosis (i.e., diagnosis >7 days after patient admission or >30 days after onset of symptoms) results in poor prognosis compared with early diagnosis.
Conclusions
Improving awareness and shortening diagnosis time may improve the prognosis of mucormycosis. If mucormycosis is suspected, appropriate samples should be collected as soon as possible and submitted for biopsy, culture, or mNGS to confirm the diagnosis.
Patient 8 was admitted to the hospital because of a cough and sputum for 3 days. Bronchoscopy was performed, and bronchoalveolar lavage fluid (BALF) was used for culture and mNGS. BALF mNGS revealed Rhizopus, and sputum fungal culture revealed a small amount of Rhizopus. Lung computed tomography (CT) changes in patient 8 from admission (October 12, 2021) to the first follow‐up after discharge (January 21, 2022) are shown in Figure 1. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9396201</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2705225119</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4258-caa8e2aedfe52fe8ec7abd2d0b9587d981f9b2126051a2c211340a71ac4bf8993</originalsourceid><addsrcrecordid>eNp9kUtPwzAQhC0EouVx4RdE4oKQAvYmTmwOSFXFU0Vc4Gw5zgZcJXGxk6L-e1JaIcGB0x7229HMDiEnjF4wSuFybmp9ASkXYoeMGZUiBgF8l4ypEHksKEtG5CCEOaVUSJbtk1HCcwmUiTF5eOrrzi5qjEqr31oXOmuiBrt3V4aocj5qeuN8szIu2HAVTSKPnXdhgaazS4yMDhgF9BbDEdmrdB3weDsPyevtzcv0Pp493z1MJ7PYpMBFbLQWCBrLCjlUKNDkuiihpIXkIi-lYJUsgEFGOdNggLEkpTpn2qRFJaRMDsn1RnfRFw2WBtvO61otvG20Xymnrfq9ae27enNLJROZDaEHgbOtgHcfPYZONTYYrGvdouuDgkzwNM3zNBvQ0z_o3PW-HeIpyCkH4IytHZ1vKDN8JnisfswwqtYNqXVD6ruhAWYb-NPWuPqHVI_T2WRz8wVjd5NI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2705225119</pqid></control><display><type>article</type><title>Multiple diagnostic methods for mucormycosis: A retrospective case series</title><source>Wiley-Blackwell Open Access Titles</source><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Wang, JiaXin ; Wang, YaoMin ; Han, Fei ; Chen, JiangHua</creator><creatorcontrib>Wang, JiaXin ; Wang, YaoMin ; Han, Fei ; Chen, JiangHua</creatorcontrib><description>Background
Mucormycosis is a rare invasive fungal disease with high mortality. Early diagnosis and targeted drugs are crucial to improving clinical outcomes.
Methods
We searched the electronic hospital database of the First Affiliated Hospital of Zhejiang University School of Medicine for adult patients with mucormycosis between 2000 and 2021. Demographic, clinical, treatment, and outcome data were collected and compared with the data in the relevant literature.
Results
Eleven cases of mucormycosis—four of multisite infection, one of skin infection, five of lung infection, and one of gastrointestinal infection—were found and analyzed. The patients were diagnosed mainly based on pathological and histological findings, and three patients had metagenomic next‐generation sequencing findings. Delayed diagnosis (i.e., diagnosis >7 days after patient admission or >30 days after onset of symptoms) results in poor prognosis compared with early diagnosis.
Conclusions
Improving awareness and shortening diagnosis time may improve the prognosis of mucormycosis. If mucormycosis is suspected, appropriate samples should be collected as soon as possible and submitted for biopsy, culture, or mNGS to confirm the diagnosis.
Patient 8 was admitted to the hospital because of a cough and sputum for 3 days. Bronchoscopy was performed, and bronchoalveolar lavage fluid (BALF) was used for culture and mNGS. BALF mNGS revealed Rhizopus, and sputum fungal culture revealed a small amount of Rhizopus. Lung computed tomography (CT) changes in patient 8 from admission (October 12, 2021) to the first follow‐up after discharge (January 21, 2022) are shown in Figure 1.</description><identifier>ISSN: 0887-8013</identifier><identifier>EISSN: 1098-2825</identifier><identifier>DOI: 10.1002/jcla.24588</identifier><identifier>PMID: 35792018</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Biopsy ; Bronchopulmonary infection ; Cancer therapies ; Chemotherapy ; Clinical outcomes ; culture ; Diabetes ; Diagnosis ; early diagnosis ; Fungal infections ; Kidney transplants ; metagenomic next‐generation sequencing (mNGS) ; Metagenomics ; Mucormycosis ; Patients ; Prognosis ; Tomography ; Tuberculosis</subject><ispartof>Journal of clinical laboratory analysis, 2022-08, Vol.36 (8), p.e24588-n/a</ispartof><rights>2022 The Authors. published by Wiley Periodicals LLC.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/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><citedby>FETCH-LOGICAL-c4258-caa8e2aedfe52fe8ec7abd2d0b9587d981f9b2126051a2c211340a71ac4bf8993</citedby><cites>FETCH-LOGICAL-c4258-caa8e2aedfe52fe8ec7abd2d0b9587d981f9b2126051a2c211340a71ac4bf8993</cites><orcidid>0000-0002-9062-3097</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2705225119/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2705225119?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11560,25751,27922,27923,37010,37011,44588,46050,46474,53789,53791,74896</link.rule.ids></links><search><creatorcontrib>Wang, JiaXin</creatorcontrib><creatorcontrib>Wang, YaoMin</creatorcontrib><creatorcontrib>Han, Fei</creatorcontrib><creatorcontrib>Chen, JiangHua</creatorcontrib><title>Multiple diagnostic methods for mucormycosis: A retrospective case series</title><title>Journal of clinical laboratory analysis</title><description>Background
Mucormycosis is a rare invasive fungal disease with high mortality. Early diagnosis and targeted drugs are crucial to improving clinical outcomes.
Methods
We searched the electronic hospital database of the First Affiliated Hospital of Zhejiang University School of Medicine for adult patients with mucormycosis between 2000 and 2021. Demographic, clinical, treatment, and outcome data were collected and compared with the data in the relevant literature.
Results
Eleven cases of mucormycosis—four of multisite infection, one of skin infection, five of lung infection, and one of gastrointestinal infection—were found and analyzed. The patients were diagnosed mainly based on pathological and histological findings, and three patients had metagenomic next‐generation sequencing findings. Delayed diagnosis (i.e., diagnosis >7 days after patient admission or >30 days after onset of symptoms) results in poor prognosis compared with early diagnosis.
Conclusions
Improving awareness and shortening diagnosis time may improve the prognosis of mucormycosis. If mucormycosis is suspected, appropriate samples should be collected as soon as possible and submitted for biopsy, culture, or mNGS to confirm the diagnosis.
Patient 8 was admitted to the hospital because of a cough and sputum for 3 days. Bronchoscopy was performed, and bronchoalveolar lavage fluid (BALF) was used for culture and mNGS. BALF mNGS revealed Rhizopus, and sputum fungal culture revealed a small amount of Rhizopus. Lung computed tomography (CT) changes in patient 8 from admission (October 12, 2021) to the first follow‐up after discharge (January 21, 2022) are shown in Figure 1.</description><subject>Biopsy</subject><subject>Bronchopulmonary infection</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Clinical outcomes</subject><subject>culture</subject><subject>Diabetes</subject><subject>Diagnosis</subject><subject>early diagnosis</subject><subject>Fungal infections</subject><subject>Kidney transplants</subject><subject>metagenomic next‐generation sequencing (mNGS)</subject><subject>Metagenomics</subject><subject>Mucormycosis</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Tomography</subject><subject>Tuberculosis</subject><issn>0887-8013</issn><issn>1098-2825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp9kUtPwzAQhC0EouVx4RdE4oKQAvYmTmwOSFXFU0Vc4Gw5zgZcJXGxk6L-e1JaIcGB0x7229HMDiEnjF4wSuFybmp9ASkXYoeMGZUiBgF8l4ypEHksKEtG5CCEOaVUSJbtk1HCcwmUiTF5eOrrzi5qjEqr31oXOmuiBrt3V4aocj5qeuN8szIu2HAVTSKPnXdhgaazS4yMDhgF9BbDEdmrdB3weDsPyevtzcv0Pp493z1MJ7PYpMBFbLQWCBrLCjlUKNDkuiihpIXkIi-lYJUsgEFGOdNggLEkpTpn2qRFJaRMDsn1RnfRFw2WBtvO61otvG20Xymnrfq9ae27enNLJROZDaEHgbOtgHcfPYZONTYYrGvdouuDgkzwNM3zNBvQ0z_o3PW-HeIpyCkH4IytHZ1vKDN8JnisfswwqtYNqXVD6ruhAWYb-NPWuPqHVI_T2WRz8wVjd5NI</recordid><startdate>202208</startdate><enddate>202208</enddate><creator>Wang, JiaXin</creator><creator>Wang, YaoMin</creator><creator>Han, Fei</creator><creator>Chen, JiangHua</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8C1</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>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9062-3097</orcidid></search><sort><creationdate>202208</creationdate><title>Multiple diagnostic methods for mucormycosis: A retrospective case series</title><author>Wang, JiaXin ; Wang, YaoMin ; Han, Fei ; Chen, JiangHua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4258-caa8e2aedfe52fe8ec7abd2d0b9587d981f9b2126051a2c211340a71ac4bf8993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biopsy</topic><topic>Bronchopulmonary infection</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Clinical outcomes</topic><topic>culture</topic><topic>Diabetes</topic><topic>Diagnosis</topic><topic>early diagnosis</topic><topic>Fungal infections</topic><topic>Kidney transplants</topic><topic>metagenomic next‐generation sequencing (mNGS)</topic><topic>Metagenomics</topic><topic>Mucormycosis</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Tomography</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, JiaXin</creatorcontrib><creatorcontrib>Wang, YaoMin</creatorcontrib><creatorcontrib>Han, Fei</creatorcontrib><creatorcontrib>Chen, JiangHua</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Online Library Free Content</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech 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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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 Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical laboratory analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, JiaXin</au><au>Wang, YaoMin</au><au>Han, Fei</au><au>Chen, JiangHua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple diagnostic methods for mucormycosis: A retrospective case series</atitle><jtitle>Journal of clinical laboratory analysis</jtitle><date>2022-08</date><risdate>2022</risdate><volume>36</volume><issue>8</issue><spage>e24588</spage><epage>n/a</epage><pages>e24588-n/a</pages><issn>0887-8013</issn><eissn>1098-2825</eissn><abstract>Background
Mucormycosis is a rare invasive fungal disease with high mortality. Early diagnosis and targeted drugs are crucial to improving clinical outcomes.
Methods
We searched the electronic hospital database of the First Affiliated Hospital of Zhejiang University School of Medicine for adult patients with mucormycosis between 2000 and 2021. Demographic, clinical, treatment, and outcome data were collected and compared with the data in the relevant literature.
Results
Eleven cases of mucormycosis—four of multisite infection, one of skin infection, five of lung infection, and one of gastrointestinal infection—were found and analyzed. The patients were diagnosed mainly based on pathological and histological findings, and three patients had metagenomic next‐generation sequencing findings. Delayed diagnosis (i.e., diagnosis >7 days after patient admission or >30 days after onset of symptoms) results in poor prognosis compared with early diagnosis.
Conclusions
Improving awareness and shortening diagnosis time may improve the prognosis of mucormycosis. If mucormycosis is suspected, appropriate samples should be collected as soon as possible and submitted for biopsy, culture, or mNGS to confirm the diagnosis.
Patient 8 was admitted to the hospital because of a cough and sputum for 3 days. Bronchoscopy was performed, and bronchoalveolar lavage fluid (BALF) was used for culture and mNGS. BALF mNGS revealed Rhizopus, and sputum fungal culture revealed a small amount of Rhizopus. Lung computed tomography (CT) changes in patient 8 from admission (October 12, 2021) to the first follow‐up after discharge (January 21, 2022) are shown in Figure 1.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>35792018</pmid><doi>10.1002/jcla.24588</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-9062-3097</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Bronchopulmonary infection Cancer therapies Chemotherapy Clinical outcomes culture Diabetes Diagnosis early diagnosis Fungal infections Kidney transplants metagenomic next‐generation sequencing (mNGS) Metagenomics Mucormycosis Patients Prognosis Tomography Tuberculosis |
title | Multiple diagnostic methods for mucormycosis: A retrospective case series |
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