Application of 18F-FDG PET/CT in Langerhans Cell Histiocytosis
Purpose. This study aims to explore the application value of the 18F-FDG PET/CT imaging in diagnosing, staging, and typing Langerhans cell histiocytosis (LCH) via the morphological and metabolic analyses of the 18F-FDG PET/CT images. Methods. We retrospectively analyzed the 18F-FDG PET/CT images and...
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description | Purpose. This study aims to explore the application value of the 18F-FDG PET/CT imaging in diagnosing, staging, and typing Langerhans cell histiocytosis (LCH) via the morphological and metabolic analyses of the 18F-FDG PET/CT images. Methods. We retrospectively analyzed the 18F-FDG PET/CT images and clinical data of nineteen patients with LCH. The shape, size, density, distribution, and 18F-FDG uptake of all lesions were documented. In addition, the SUVmax of the lesions, liver, and blood pool was measured prior to calculating the lesion-to-liver and lesion-to-blood pool ratios. Results. Among the 19 analyzed patients, the positive rate of the PET/CT image was 94.7% (18/19), with 1 false negative (5.3%, 1/19) case occurring in the cutaneous LCH. Among the 76 lesions, 69 were FDG-avid lesions (69/76, 90.8%). Additionally, we observed no FDG uptake in 7 lesions (7/76, 9.2%). In contrast, 59 lesions (59/76, 77.6%) were abnormal on diagnostic CT scan, but 17 lesions (17/76, 22.4%) were undetected. The 18F-FDG PET/CT image revealed additional 6 lesions in the bone, 4 in the lymph node, 3 in the spleen, and 3 occult lesions, which CT scan did not detect. Additionally, there were 6 cases with single-system LCH. The remaining 13 cases were multisystem LCH. Our 18F-FDG PET/CT image analyses altered the typing of 4 LCH patients. In the case of all lesions, the mean SUVmax of the 18F-FDG-avid lesions was 5.4 ± 5.1 (range, 0.8∼26.2), and the mean lesion-to-liver SUVmax ratio was 3.1 ± 2.52 (range, 0.7∼11.9), and the mean lesion-to-blood pool SUVmax ratio was 4.6 ± 3.4 (range 0.7∼17.5). Conclusion. The 18F-FDG PET/CT image plays an essential role in LCH diagnosis, primary staging, and typing. It can accurately evaluate the distribution, range, and metabolic information of LCH, providing a vital imaging basis for the clinical evaluation of disease conditions, selection of treatment schemes, and determining patient prognosis. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9417783</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2709735669</sourcerecordid><originalsourceid>FETCH-LOGICAL-c290t-b7b9d3277f6236041ca65bdbe7c4a5723f81fca305f94f39b7167fd2ac0b4f3b3</originalsourceid><addsrcrecordid>eNpVkF1LwzAUhoMobk7v_AG9FKQuyWma5mYw6j6EgV7M65CkyRbp2tp0yv69HRsDr87Xw_tyXoQeCX4hhLExxZSOM8gYAL1Cw37F4gQIv770WAzQXQhfGCcJCLhFA0gxIwLIEE2mTVN6ozpfV1HtIpLN4_nrIvqYrcf5OvJVtFLVxrZbVYUot2UZLX3oYXPo6uDDPbpxqgz24VxH6HM-W-fLePW-eMunq9hQgbtYcy0KoJy7lPbeCTEqZbrQlptEMU7BZcQZBZg5kTgQmpOUu4Iqg3U_axihyUm32eudLYytulaVsmn9TrUHWSsv_18qv5Wb-keKhHCeQS_wdBZo6--9DZ3c-WD6f1Rl632QlGPBgaWp6NHnE7r1VaF-_cWFYHlMXB4Tl-fE4Q_k8XAe</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2709735669</pqid></control><display><type>article</type><title>Application of 18F-FDG PET/CT in Langerhans Cell Histiocytosis</title><source>EZB Free E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>PubMed Central Open Access</source><creator>Liao, Fengxiang ; Luo, Zhehuang ; Huang, Zizhen ; Xu, Rong ; Qi, Wanling ; Shao, Mingyan ; Lei, Pinggui ; Fan, Bing</creator><contributor>Vali, Reza</contributor><creatorcontrib>Liao, Fengxiang ; Luo, Zhehuang ; Huang, Zizhen ; Xu, Rong ; Qi, Wanling ; Shao, Mingyan ; Lei, Pinggui ; Fan, Bing ; Vali, Reza</creatorcontrib><description>Purpose. This study aims to explore the application value of the 18F-FDG PET/CT imaging in diagnosing, staging, and typing Langerhans cell histiocytosis (LCH) via the morphological and metabolic analyses of the 18F-FDG PET/CT images. Methods. We retrospectively analyzed the 18F-FDG PET/CT images and clinical data of nineteen patients with LCH. The shape, size, density, distribution, and 18F-FDG uptake of all lesions were documented. In addition, the SUVmax of the lesions, liver, and blood pool was measured prior to calculating the lesion-to-liver and lesion-to-blood pool ratios. Results. Among the 19 analyzed patients, the positive rate of the PET/CT image was 94.7% (18/19), with 1 false negative (5.3%, 1/19) case occurring in the cutaneous LCH. Among the 76 lesions, 69 were FDG-avid lesions (69/76, 90.8%). Additionally, we observed no FDG uptake in 7 lesions (7/76, 9.2%). In contrast, 59 lesions (59/76, 77.6%) were abnormal on diagnostic CT scan, but 17 lesions (17/76, 22.4%) were undetected. The 18F-FDG PET/CT image revealed additional 6 lesions in the bone, 4 in the lymph node, 3 in the spleen, and 3 occult lesions, which CT scan did not detect. Additionally, there were 6 cases with single-system LCH. The remaining 13 cases were multisystem LCH. Our 18F-FDG PET/CT image analyses altered the typing of 4 LCH patients. In the case of all lesions, the mean SUVmax of the 18F-FDG-avid lesions was 5.4 ± 5.1 (range, 0.8∼26.2), and the mean lesion-to-liver SUVmax ratio was 3.1 ± 2.52 (range, 0.7∼11.9), and the mean lesion-to-blood pool SUVmax ratio was 4.6 ± 3.4 (range 0.7∼17.5). Conclusion. The 18F-FDG PET/CT image plays an essential role in LCH diagnosis, primary staging, and typing. It can accurately evaluate the distribution, range, and metabolic information of LCH, providing a vital imaging basis for the clinical evaluation of disease conditions, selection of treatment schemes, and determining patient prognosis.</description><identifier>ISSN: 1555-4309</identifier><identifier>EISSN: 1555-4317</identifier><identifier>DOI: 10.1155/2022/8385332</identifier><identifier>PMID: 36051931</identifier><language>eng</language><publisher>Hindawi</publisher><ispartof>Contrast media and molecular imaging, 2022-08, Vol.2022, p.8385332-8385332</ispartof><rights>Copyright © 2022 Fengxiang Liao et al.</rights><rights>Copyright © 2022 Fengxiang Liao et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c290t-b7b9d3277f6236041ca65bdbe7c4a5723f81fca305f94f39b7167fd2ac0b4f3b3</citedby><orcidid>0000-0003-4439-6150</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417783/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417783/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids></links><search><contributor>Vali, Reza</contributor><creatorcontrib>Liao, Fengxiang</creatorcontrib><creatorcontrib>Luo, Zhehuang</creatorcontrib><creatorcontrib>Huang, Zizhen</creatorcontrib><creatorcontrib>Xu, Rong</creatorcontrib><creatorcontrib>Qi, Wanling</creatorcontrib><creatorcontrib>Shao, Mingyan</creatorcontrib><creatorcontrib>Lei, Pinggui</creatorcontrib><creatorcontrib>Fan, Bing</creatorcontrib><title>Application of 18F-FDG PET/CT in Langerhans Cell Histiocytosis</title><title>Contrast media and molecular imaging</title><description>Purpose. This study aims to explore the application value of the 18F-FDG PET/CT imaging in diagnosing, staging, and typing Langerhans cell histiocytosis (LCH) via the morphological and metabolic analyses of the 18F-FDG PET/CT images. Methods. We retrospectively analyzed the 18F-FDG PET/CT images and clinical data of nineteen patients with LCH. The shape, size, density, distribution, and 18F-FDG uptake of all lesions were documented. In addition, the SUVmax of the lesions, liver, and blood pool was measured prior to calculating the lesion-to-liver and lesion-to-blood pool ratios. Results. Among the 19 analyzed patients, the positive rate of the PET/CT image was 94.7% (18/19), with 1 false negative (5.3%, 1/19) case occurring in the cutaneous LCH. Among the 76 lesions, 69 were FDG-avid lesions (69/76, 90.8%). Additionally, we observed no FDG uptake in 7 lesions (7/76, 9.2%). In contrast, 59 lesions (59/76, 77.6%) were abnormal on diagnostic CT scan, but 17 lesions (17/76, 22.4%) were undetected. The 18F-FDG PET/CT image revealed additional 6 lesions in the bone, 4 in the lymph node, 3 in the spleen, and 3 occult lesions, which CT scan did not detect. Additionally, there were 6 cases with single-system LCH. The remaining 13 cases were multisystem LCH. Our 18F-FDG PET/CT image analyses altered the typing of 4 LCH patients. In the case of all lesions, the mean SUVmax of the 18F-FDG-avid lesions was 5.4 ± 5.1 (range, 0.8∼26.2), and the mean lesion-to-liver SUVmax ratio was 3.1 ± 2.52 (range, 0.7∼11.9), and the mean lesion-to-blood pool SUVmax ratio was 4.6 ± 3.4 (range 0.7∼17.5). Conclusion. The 18F-FDG PET/CT image plays an essential role in LCH diagnosis, primary staging, and typing. It can accurately evaluate the distribution, range, and metabolic information of LCH, providing a vital imaging basis for the clinical evaluation of disease conditions, selection of treatment schemes, and determining patient prognosis.</description><issn>1555-4309</issn><issn>1555-4317</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><recordid>eNpVkF1LwzAUhoMobk7v_AG9FKQuyWma5mYw6j6EgV7M65CkyRbp2tp0yv69HRsDr87Xw_tyXoQeCX4hhLExxZSOM8gYAL1Cw37F4gQIv770WAzQXQhfGCcJCLhFA0gxIwLIEE2mTVN6ozpfV1HtIpLN4_nrIvqYrcf5OvJVtFLVxrZbVYUot2UZLX3oYXPo6uDDPbpxqgz24VxH6HM-W-fLePW-eMunq9hQgbtYcy0KoJy7lPbeCTEqZbrQlptEMU7BZcQZBZg5kTgQmpOUu4Iqg3U_axihyUm32eudLYytulaVsmn9TrUHWSsv_18qv5Wb-keKhHCeQS_wdBZo6--9DZ3c-WD6f1Rl632QlGPBgaWp6NHnE7r1VaF-_cWFYHlMXB4Tl-fE4Q_k8XAe</recordid><startdate>20220819</startdate><enddate>20220819</enddate><creator>Liao, Fengxiang</creator><creator>Luo, Zhehuang</creator><creator>Huang, Zizhen</creator><creator>Xu, Rong</creator><creator>Qi, Wanling</creator><creator>Shao, Mingyan</creator><creator>Lei, Pinggui</creator><creator>Fan, Bing</creator><general>Hindawi</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4439-6150</orcidid></search><sort><creationdate>20220819</creationdate><title>Application of 18F-FDG PET/CT in Langerhans Cell Histiocytosis</title><author>Liao, Fengxiang ; Luo, Zhehuang ; Huang, Zizhen ; Xu, Rong ; Qi, Wanling ; Shao, Mingyan ; Lei, Pinggui ; Fan, Bing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c290t-b7b9d3277f6236041ca65bdbe7c4a5723f81fca305f94f39b7167fd2ac0b4f3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liao, Fengxiang</creatorcontrib><creatorcontrib>Luo, Zhehuang</creatorcontrib><creatorcontrib>Huang, Zizhen</creatorcontrib><creatorcontrib>Xu, Rong</creatorcontrib><creatorcontrib>Qi, Wanling</creatorcontrib><creatorcontrib>Shao, Mingyan</creatorcontrib><creatorcontrib>Lei, Pinggui</creatorcontrib><creatorcontrib>Fan, Bing</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Contrast media and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liao, Fengxiang</au><au>Luo, Zhehuang</au><au>Huang, Zizhen</au><au>Xu, Rong</au><au>Qi, Wanling</au><au>Shao, Mingyan</au><au>Lei, Pinggui</au><au>Fan, Bing</au><au>Vali, Reza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of 18F-FDG PET/CT in Langerhans Cell Histiocytosis</atitle><jtitle>Contrast media and molecular imaging</jtitle><date>2022-08-19</date><risdate>2022</risdate><volume>2022</volume><spage>8385332</spage><epage>8385332</epage><pages>8385332-8385332</pages><issn>1555-4309</issn><eissn>1555-4317</eissn><abstract>Purpose. This study aims to explore the application value of the 18F-FDG PET/CT imaging in diagnosing, staging, and typing Langerhans cell histiocytosis (LCH) via the morphological and metabolic analyses of the 18F-FDG PET/CT images. Methods. We retrospectively analyzed the 18F-FDG PET/CT images and clinical data of nineteen patients with LCH. The shape, size, density, distribution, and 18F-FDG uptake of all lesions were documented. In addition, the SUVmax of the lesions, liver, and blood pool was measured prior to calculating the lesion-to-liver and lesion-to-blood pool ratios. Results. Among the 19 analyzed patients, the positive rate of the PET/CT image was 94.7% (18/19), with 1 false negative (5.3%, 1/19) case occurring in the cutaneous LCH. Among the 76 lesions, 69 were FDG-avid lesions (69/76, 90.8%). Additionally, we observed no FDG uptake in 7 lesions (7/76, 9.2%). In contrast, 59 lesions (59/76, 77.6%) were abnormal on diagnostic CT scan, but 17 lesions (17/76, 22.4%) were undetected. The 18F-FDG PET/CT image revealed additional 6 lesions in the bone, 4 in the lymph node, 3 in the spleen, and 3 occult lesions, which CT scan did not detect. Additionally, there were 6 cases with single-system LCH. The remaining 13 cases were multisystem LCH. Our 18F-FDG PET/CT image analyses altered the typing of 4 LCH patients. In the case of all lesions, the mean SUVmax of the 18F-FDG-avid lesions was 5.4 ± 5.1 (range, 0.8∼26.2), and the mean lesion-to-liver SUVmax ratio was 3.1 ± 2.52 (range, 0.7∼11.9), and the mean lesion-to-blood pool SUVmax ratio was 4.6 ± 3.4 (range 0.7∼17.5). Conclusion. The 18F-FDG PET/CT image plays an essential role in LCH diagnosis, primary staging, and typing. It can accurately evaluate the distribution, range, and metabolic information of LCH, providing a vital imaging basis for the clinical evaluation of disease conditions, selection of treatment schemes, and determining patient prognosis.</abstract><pub>Hindawi</pub><pmid>36051931</pmid><doi>10.1155/2022/8385332</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-4439-6150</orcidid><oa>free_for_read</oa></addata></record> |
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title | Application of 18F-FDG PET/CT in Langerhans Cell Histiocytosis |
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