罕见的头皮毛窦1例。

IF 1.1 Q4 ONCOLOGY
International journal of clinical and experimental pathology Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.62347/QIVB9496
Xindong Wu
{"title":"罕见的头皮毛窦1例。","authors":"Xindong Wu","doi":"10.62347/QIVB9496","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Pilonidal sinus is a chronic inflammatory condition that typically occurs in the sacrococcygeal region and rarely in other locations. Scalp pilonidal sinus is extremely uncommon, making this case noteworthy as it expands the differential diagnosis for scalp nodular lesions.</p><p><strong>Case presentation: </strong>A 16-year-old girl presented with a persistent fluid-draining nodule on the top of her head, present for over a decade. She had a history of scalp injury at birth. Examination revealed a 1×2 cm mobile, tough nodule with a central opening and sparse surrounding hair. Imaging showed a gas density under the scalp but no bone involvement. The nodule was surgically excised. Histopathology confirmed pilonidal sinus, showing embedded hair, sebaceous gland involvement, and inflammatory cell infiltration. The patient recovered fully, with no recurrence or complications during three years of follow-up.</p><p><strong>Conclusions: </strong>This rare case of pilonidal sinus on the scalp highlights the importance of considering it in the differential diagnosis of scalp nodular lesions, particularly in patients with a history of trauma. It emphasizes the need for surgical treatment and careful follow-up to prevent recurrence.</p>","PeriodicalId":13943,"journal":{"name":"International journal of clinical and experimental pathology","volume":"18 5","pages":"199-202"},"PeriodicalIF":1.1000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12163481/pdf/","citationCount":"0","resultStr":"{\"title\":\"Rare case of pilonidal sinus of scalp: a case report.\",\"authors\":\"Xindong Wu\",\"doi\":\"10.62347/QIVB9496\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Pilonidal sinus is a chronic inflammatory condition that typically occurs in the sacrococcygeal region and rarely in other locations. Scalp pilonidal sinus is extremely uncommon, making this case noteworthy as it expands the differential diagnosis for scalp nodular lesions.</p><p><strong>Case presentation: </strong>A 16-year-old girl presented with a persistent fluid-draining nodule on the top of her head, present for over a decade. She had a history of scalp injury at birth. Examination revealed a 1×2 cm mobile, tough nodule with a central opening and sparse surrounding hair. Imaging showed a gas density under the scalp but no bone involvement. The nodule was surgically excised. Histopathology confirmed pilonidal sinus, showing embedded hair, sebaceous gland involvement, and inflammatory cell infiltration. The patient recovered fully, with no recurrence or complications during three years of follow-up.</p><p><strong>Conclusions: </strong>This rare case of pilonidal sinus on the scalp highlights the importance of considering it in the differential diagnosis of scalp nodular lesions, particularly in patients with a history of trauma. It emphasizes the need for surgical treatment and careful follow-up to prevent recurrence.</p>\",\"PeriodicalId\":13943,\"journal\":{\"name\":\"International journal of clinical and experimental pathology\",\"volume\":\"18 5\",\"pages\":\"199-202\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2025-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12163481/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of clinical and experimental pathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.62347/QIVB9496\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of clinical and experimental pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.62347/QIVB9496","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:毛突窦是一种慢性炎症,通常发生在骶尾骨区,很少发生在其他部位。头皮毛突窦是非常罕见的,使得这个病例值得注意,因为它扩大了头皮结节性病变的鉴别诊断。病例介绍:一名16岁的女孩,在她的头顶出现了一个持续的液体引流结节,已经存在了十多年。她出生时有头皮损伤史。检查发现一个1×2厘米大小的移动结节,有中心开口,周围毛发稀疏。影像显示头皮下有气体密度,但未累及骨骼。手术切除了结节。组织病理学证实为毛突窦,显示毛发嵌埋,皮脂腺受累,炎症细胞浸润。患者完全恢复,随访3年无复发或并发症。结论:这一罕见的头皮毛突窦病例强调了在头皮结节性病变的鉴别诊断中考虑它的重要性,特别是在有创伤史的患者中。它强调需要手术治疗和仔细的随访,以防止复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare case of pilonidal sinus of scalp: a case report.

Background: Pilonidal sinus is a chronic inflammatory condition that typically occurs in the sacrococcygeal region and rarely in other locations. Scalp pilonidal sinus is extremely uncommon, making this case noteworthy as it expands the differential diagnosis for scalp nodular lesions.

Case presentation: A 16-year-old girl presented with a persistent fluid-draining nodule on the top of her head, present for over a decade. She had a history of scalp injury at birth. Examination revealed a 1×2 cm mobile, tough nodule with a central opening and sparse surrounding hair. Imaging showed a gas density under the scalp but no bone involvement. The nodule was surgically excised. Histopathology confirmed pilonidal sinus, showing embedded hair, sebaceous gland involvement, and inflammatory cell infiltration. The patient recovered fully, with no recurrence or complications during three years of follow-up.

Conclusions: This rare case of pilonidal sinus on the scalp highlights the importance of considering it in the differential diagnosis of scalp nodular lesions, particularly in patients with a history of trauma. It emphasizes the need for surgical treatment and careful follow-up to prevent recurrence.

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
42
审稿时长
1 months
期刊介绍: The International Journal of Clinical and Experimental Pathology (IJCEP, ISSN 1936-2625) is a peer reviewed, open access online journal. It was founded in 2008 by an international group of academic pathologists and scientists who are devoted to the scientific exploration of human disease and the rapid dissemination of original data. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal.
×
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:604180095
Book学术官方微信