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融合性网状乳头瘤病诊断中的挑战:一例非典型病变分布病例

Challenges in diagnosing confluent and reticulated papillomatosis: a case of atypical lesions distribution.

作者信息

Alsadi Mohammad Obada, Alghali Dalia, Zoghpy Ayah, Haddad Sultaneh, Jwainat Mu'taz, Jawad Hanan, Almaghoush Reshdy, Zeeb Doha, Eysa Nour Alhoda, Alsaghir Nemat

机构信息

Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.

Faculty of Medicine, University of Tatrous, Tartous, Syrian Arab Republic.

出版信息

Oxf Med Case Reports. 2025 Aug 20;2025(8):omaf142. doi: 10.1093/omcr/omaf142. eCollection 2025 Aug.

DOI:10.1093/omcr/omaf142
PMID:40843048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12365960/
Abstract

Gougerot-Carteaud Syndrome (Confluent and Reticulate Papillomatosis, CARP) is a rare dermatological condition characterized by coalescent reticulate papules predominantly affecting the upper trunk and neck. The etiology remains debated, with hypotheses ranging from keratinization disorders to bacterial and fungal infections, endocrine abnormalities, and genetic predispositions. This report presents the case of an 18-year-old male with pruritic, maculopapular, and scaly lesions unresponsive to antifungal and antibiotic therapies. Histopathological examination revealed hyperkeratosis, acanthosis, and papillomatosis, leading to a diagnosis of CARP. Despite initial treatment with doxycycline, the patient showed significant improvement only after isotretinoin therapy, suggesting a non-bacterial etiology. The consanguinity in the patient's family underscores the potential for genetic factors in CARP's pathogenesis. This case highlights the diagnostic and therapeutic challenges associated with CARP and emphasizes the need for further research into its underlying mechanisms.

摘要

Gougerot-Carteaud综合征(融合性网状乳头瘤病,CARP)是一种罕见的皮肤病,其特征为融合性网状丘疹,主要累及上躯干和颈部。病因仍存在争议,假说范围从角化异常到细菌和真菌感染、内分泌异常以及遗传易感性。本报告介绍了一名18岁男性病例,其患有瘙痒性斑丘疹和鳞屑性损害,对抗真菌和抗生素治疗无反应。组织病理学检查显示角化过度、棘层肥厚和乳头瘤样增生,从而诊断为CARP。尽管最初用强力霉素治疗,但患者仅在异维A酸治疗后才显示出显著改善,提示非细菌性病因。患者家族中的近亲关系凸显了遗传因素在CARP发病机制中的可能性。该病例突出了与CARP相关的诊断和治疗挑战,并强调需要对其潜在机制进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/a1dd4604a55d/omaf142f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/2468331ed598/omaf142f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/880f6140b627/omaf142f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/a1dd4604a55d/omaf142f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/2468331ed598/omaf142f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/880f6140b627/omaf142f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d54/12365960/a1dd4604a55d/omaf142f3.jpg

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本文引用的文献

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Confluent and Reticulated Papillomatosis Resembling Pityriasis Versicolor and Acanthosis Nigricans: Case Report.类似花斑癣和黑棘皮病的融合性网状乳头瘤病:病例报告
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2
Tinea versicolor: an updated review.花斑糠疹:最新综述
Drugs Context. 2022 Nov 14;11. doi: 10.7573/dic.2022-9-2. eCollection 2022.
3
Confluent and Reticulated Papillomatosis of Gougerot and Carteaud: A Case Report and Review of the Literature.古热罗和卡托网状融合性乳头瘤病:一例报告及文献复习
Cureus. 2022 Apr 28;14(4):e24557. doi: 10.7759/cureus.24557. eCollection 2022 Apr.
4
Familial Confluent and Reticulated Papillomatosis in 2 Kindreds Including 3 Generations.两个家族三代人中的家族性融合性网状乳头瘤病
J Cutan Med Surg. 2018 May/Jun;22(3):330-332. doi: 10.1177/1203475417738968. Epub 2018 Apr 22.
5
Polycystic Ovarian Syndrome-associated Confluent and Reticulated Papillomatosis: Report of a Patient Successfully Treated with Azithromycin.多囊卵巢综合征相关的融合性网状乳头瘤病:阿奇霉素成功治疗1例报告
J Clin Aesthet Dermatol. 2017 Sep;10(9):30-35. Epub 2017 Sep 1.
6
Updated diagnosis criteria for confluent and reticulated papillomatosis: a case report.融合性网状乳头瘤病的更新诊断标准:一例病例报告
Ann Dermatol. 2014 Jun;26(3):409-10. doi: 10.5021/ad.2014.26.3.409. Epub 2014 Jun 12.
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Confluent and reticulated papillomatosis: favourable response to low-dose isotretinoin.融合性网状乳头瘤病:对低剂量异维A酸反应良好。
J Eur Acad Dermatol Venereol. 2009 Nov;23(11):1342-3. doi: 10.1111/j.1468-3083.2009.03219.x. Epub 2009 Mar 11.
8
Confluent and reticulated papillomatosis : a review of the literature.融合性网状乳头瘤病:文献综述
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Br J Dermatol. 2006 Feb;154(2):287-93. doi: 10.1111/j.1365-2133.2005.06955.x.