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富含蛋白质的毛发鞘囊肿:一个潜在的诊断陷阱。

Trichilemmal cysts with proteinaceous material: A potential diagnostic pitfall.

机构信息

Department of Dermatology, Nara Medical University School of Medicine, Kashihara, Japan.

Department of Pathology, Fukuoka University School of medicine, Fukuoka, Japan.

出版信息

J Cutan Pathol. 2022 Jun;49(6):515-524. doi: 10.1111/cup.14214. Epub 2022 Feb 22.

DOI:10.1111/cup.14214
PMID:35166386
Abstract

BACKGROUND

Cysts of the skin are observed frequently and their diagnoses are generally straightforward. However, atypical cystic lesions for which differentiation is indistinct have been noted.

METHODS

We examined five cases of trichilemmal cyst with proteinaceous material (TCPM), which required differentiation from sweat duct/gland tumors. We investigated the histopathological findings of TCPMs and evaluated the immunohistochemical expression of cytokeratin (CK) 10, CK13, CK17, CK19, CD8, and CD117. Immunohistochemical analysis was performed on the 5 TCPMs, 10 trichilemmal cysts (TCs), 5 clear-cell hidradenomas, 5 poroid hidradenomas, and cutaneous normal adnexa.

RESULTS

Apoptotic cells were present in the cyst wall with a small amount of keratin or calcification in the cavity of TCPMs. The TCPMs and TCs were negative for CK19 and CD117, on the other hand clear-cell hidradenoma and poroid hidradenoma were positive for CK19 and CD117. The restricted positivity for CK10 was detected in the suprabasal layers of the cyst walls of TCPMs and TCs. The immunostaining patterns of TCPMs and TCs were similar to those of normal follicular isthmus.

CONCLUSIONS

The histopathological findings with characteristics of TCs and a panel of immunohistochemical antibodies including CD117, CK19, and CK10 contributed to a correct diagnosis of TCPM.

摘要

背景

皮肤囊肿较为常见,其诊断通常较为直接。然而,也存在一些鉴别困难的非典型囊性病变。

方法

我们研究了 5 例伴有蛋白样物质的毛鞘囊肿(TCPM),这些病例需要与汗腺/腺肿瘤相鉴别。我们分析了 TCPM 的组织病理学特征,并评估了细胞角蛋白(CK)10、CK13、CK17、CK19、CD8 和 CD117 的免疫组化表达。对 5 例 TCPM、10 例毛鞘囊肿(TCs)、5 例透明细胞汗腺瘤、5 例小汗腺汗腺瘤和皮肤正常附件进行了免疫组化分析。

结果

TCPM 的囊壁可见凋亡细胞,腔内有少量角蛋白或钙化。TCPM 和 TCs 对 CK19 和 CD117 均为阴性,而透明细胞汗腺瘤和小汗腺汗腺瘤则对 CK19 和 CD117 均为阳性。TCPM 和 TCs 的囊壁的基底层有 CK10 的局灶性阳性。TCPM 和 TCs 的免疫组化模式与正常滤泡峡部相似。

结论

TCs 的组织病理学特征和包括 CD117、CK19 和 CK10 在内的一组免疫组化抗体有助于正确诊断 TCPM。

相似文献

1
Trichilemmal cysts with proteinaceous material: A potential diagnostic pitfall.富含蛋白质的毛发鞘囊肿:一个潜在的诊断陷阱。
J Cutan Pathol. 2022 Jun;49(6):515-524. doi: 10.1111/cup.14214. Epub 2022 Feb 22.
2
A single lesion demonstrating features of eccrine poroma and poroid hidradenoma.一个显示小汗腺汗孔瘤和类汗腺瘤特征的单一病变。
J Dermatol. 1995 Oct;22(10):773-9. doi: 10.1111/j.1346-8138.1995.tb03920.x.
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A case of cystic dermal duct tumor corresponding to poroid hidradenoma.一例与汗管瘤样汗腺瘤相对应的囊性皮肤导管瘤。
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Cytokeratin expression of apocrine and eccrine poromas with special reference to its expression in cuticular cells.顶泌汗腺汗孔瘤和小汗腺汗孔瘤的细胞角蛋白表达,特别提及在角质形成细胞中的表达。
J Cutan Pathol. 2000 Aug;27(7):367-73. doi: 10.1034/j.1600-0560.2000.027007367.x.
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Proliferating trichilemmal cyst: a simulant of squamous cell carcinoma.增殖性外毛根鞘囊肿:一种鳞状细胞癌的模拟物。
Cancer. 1981 Sep 1;48(5):1207-14. doi: 10.1002/1097-0142(19810901)48:5<1207::aid-cncr2820480526>3.0.co;2-1.
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Eccrine poroma: a review of the literature and discussion of six personal cases.小汗腺汗孔瘤:文献综述及6例个人病例讨论
Aust J Dermatol. 1961 Jun;6:59-66. doi: 10.1111/j.1440-0960.1961.tb01330.x.
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Poroid hidradenoma: a case report.多孔性汗腺瘤:一例报告
In Vivo. 2007 Sep-Oct;21(5):905-7.
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NUT Expression Is of Diagnostic Utility in the Distinction of Digital Papillary Carcinoma From Poroid Hidradenoma.NUT 表达在鉴别指状突状细胞癌与多孔性汗腺瘤中具有诊断效用。
Am J Dermatopathol. 2024 Feb 1;46(2):98-100. doi: 10.1097/DAD.0000000000002596. Epub 2023 Nov 14.
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[Poroid hidradenoma].[多孔性汗腺瘤]
Actas Dermosifiliogr. 2005 Jul-Aug;96(6):398-9. doi: 10.1016/s0001-7310(05)73100-8.
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Poroid hidradenoma: a light microscopic and immunohistochemical study.多孔性汗腺瘤:光镜与免疫组化研究
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