表面CD34阳性成纤维细胞瘤2例报告。

Jung Eun Yim, Hyeong Mok Kwon, Hye Ri Kim, Dong Hoon Shin, Jong Soo Choi, Joon Hyuk Choi, Young Kyung Bae
{"title":"表面CD34阳性成纤维细胞瘤2例报告。","authors":"Jung Eun Yim,&nbsp;Hyeong Mok Kwon,&nbsp;Hye Ri Kim,&nbsp;Dong Hoon Shin,&nbsp;Jong Soo Choi,&nbsp;Joon Hyuk Choi,&nbsp;Young Kyung Bae","doi":"10.5021/ad.20.328","DOIUrl":null,"url":null,"abstract":"<p><p>Superficial CD34-positive fibroblastic tumor (SCPFT) is a recently described disease entity characterized by marked nuclear pleomorphism, low mitotic count, and diffuse CD34 positivity. It is a rare, distinctive, low-grade fibroblastic neoplasm. To date, only 44 cases have been reported in the English-language literature. Herein, we report two cases of SCPFT involving a 48-year-old male and a 22-year-old male with superficial tumors on the right and left thighs, respectively. Excision was performed in both cases. Histologically, both tumors showed spindle-to-epithelioid cells arranged in fascicular or sheet-like patterns. Most cells displayed granular or eosinophilic glassy cytoplasm, marked nuclear pleomorphism, and a low mitotic rate. On immunohistochemical staining, tumor cells were diffusely positive for CD34 and negative for S100 protein, smooth muscle actin, and desmin. After wide excision, neither patient experienced recurrence or metastasis after 16 months and 11 months of clinical follow-up, respectively. To the best of our knowledge, these are the first two cases of SCPFT reported in Korea. We believe these case reports would contribute to the clinicopathological understanding of SCPFT and assist clinicians in differentiating this tumor from other superficial soft tissue neoplasms.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S25-S29"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a8/bf/ad-35-S25.PMC10608372.pdf","citationCount":"0","resultStr":"{\"title\":\"Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports.\",\"authors\":\"Jung Eun Yim,&nbsp;Hyeong Mok Kwon,&nbsp;Hye Ri Kim,&nbsp;Dong Hoon Shin,&nbsp;Jong Soo Choi,&nbsp;Joon Hyuk Choi,&nbsp;Young Kyung Bae\",\"doi\":\"10.5021/ad.20.328\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Superficial CD34-positive fibroblastic tumor (SCPFT) is a recently described disease entity characterized by marked nuclear pleomorphism, low mitotic count, and diffuse CD34 positivity. It is a rare, distinctive, low-grade fibroblastic neoplasm. To date, only 44 cases have been reported in the English-language literature. Herein, we report two cases of SCPFT involving a 48-year-old male and a 22-year-old male with superficial tumors on the right and left thighs, respectively. Excision was performed in both cases. Histologically, both tumors showed spindle-to-epithelioid cells arranged in fascicular or sheet-like patterns. Most cells displayed granular or eosinophilic glassy cytoplasm, marked nuclear pleomorphism, and a low mitotic rate. On immunohistochemical staining, tumor cells were diffusely positive for CD34 and negative for S100 protein, smooth muscle actin, and desmin. After wide excision, neither patient experienced recurrence or metastasis after 16 months and 11 months of clinical follow-up, respectively. To the best of our knowledge, these are the first two cases of SCPFT reported in Korea. We believe these case reports would contribute to the clinicopathological understanding of SCPFT and assist clinicians in differentiating this tumor from other superficial soft tissue neoplasms.</p>\",\"PeriodicalId\":94298,\"journal\":{\"name\":\"Annals of dermatology\",\"volume\":\"35 Suppl 1\",\"pages\":\"S25-S29\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a8/bf/ad-35-S25.PMC10608372.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of dermatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5021/ad.20.328\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5021/ad.20.328","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

表面CD34阳性纤维母细胞瘤(SCPFT)是最近描述的一种疾病,其特征是明显的核多形性、低有丝分裂计数和弥漫性CD34阳性。它是一种罕见的、独特的、低级别的成纤维细胞肿瘤。迄今为止,英文文献中只报告了44例病例。在此,我们报告了两例SCPFT,分别涉及一名48岁男性和一名22岁男性,右大腿和左大腿浅表肿瘤。两例均行切除术。组织学上,两种肿瘤均显示梭形至上皮样细胞排列成束状或片状。大多数细胞显示颗粒状或嗜酸性玻璃质细胞质,明显的细胞核多形性,有丝分裂率低。免疫组织化学染色显示,肿瘤细胞CD34呈弥漫性阳性,S100蛋白、平滑肌肌动蛋白和结蛋白呈阴性。广泛切除后,分别在16个月和11个月的临床随访后,两名患者均未出现复发或转移。据我们所知,这是韩国报告的前两例SCPFT病例。我们相信这些病例报告将有助于对SCPFT的临床病理学理解,并有助于临床医生将该肿瘤与其他浅表软组织肿瘤区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports.

Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports.

Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports.

Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports.

Superficial CD34-positive fibroblastic tumor (SCPFT) is a recently described disease entity characterized by marked nuclear pleomorphism, low mitotic count, and diffuse CD34 positivity. It is a rare, distinctive, low-grade fibroblastic neoplasm. To date, only 44 cases have been reported in the English-language literature. Herein, we report two cases of SCPFT involving a 48-year-old male and a 22-year-old male with superficial tumors on the right and left thighs, respectively. Excision was performed in both cases. Histologically, both tumors showed spindle-to-epithelioid cells arranged in fascicular or sheet-like patterns. Most cells displayed granular or eosinophilic glassy cytoplasm, marked nuclear pleomorphism, and a low mitotic rate. On immunohistochemical staining, tumor cells were diffusely positive for CD34 and negative for S100 protein, smooth muscle actin, and desmin. After wide excision, neither patient experienced recurrence or metastasis after 16 months and 11 months of clinical follow-up, respectively. To the best of our knowledge, these are the first two cases of SCPFT reported in Korea. We believe these case reports would contribute to the clinicopathological understanding of SCPFT and assist clinicians in differentiating this tumor from other superficial soft tissue neoplasms.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信