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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Veröffentlicht in:Contrast media and molecular imaging 2022-08, Vol.2022, p.8385332-8385332
Hauptverfasser: Liao, Fengxiang, Luo, Zhehuang, Huang, Zizhen, Xu, Rong, Qi, Wanling, Shao, Mingyan, Lei, Pinggui, Fan, Bing
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container_title Contrast media and molecular imaging
container_volume 2022
creator Liao, Fengxiang
Luo, Zhehuang
Huang, Zizhen
Xu, Rong
Qi, Wanling
Shao, Mingyan
Lei, Pinggui
Fan, Bing
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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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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