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Panfolliculoma is a distinctive and unusual benign follicular neoplasm. It shows differentiation towards all components of the hair follicle, including the upper and the lower segments. We report two cases of this rare disease. The first patient presented with a painful nodule on the scalp and the second patient had an asymptomatic skin-colored nodule on his left eyebrow. Histopathologic examination of both cases revealed lobular proliferation of solid-cystic follicular structures. The cystic structures contain laminated keratin, indicating infundibular differentiation. The solid tumor part was composed of basaloid germinative cells, matricial cells, and cells with trichohyalin granules, representing inner root sheath differentiation. The range of differentiations was highlighted using immunohistochemical stains, including labeling of cytokeratin 1, 5, 10, 14 (using 34bE12), cytokeratin 5/6, CD34 (outer root sheath), and Ber-EP4 (lower segment of hair follicle). Panfolliculoma should not be confused with trichofolliculoma or trichoblastoma. 相似文献
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We report a rare case of intraepidermal sebaceous carcinoma which occurred on the left upper arm of an old woman. Light-microscopic findings revealed that almost all the histopathological lesions were in the epidermis and showed pagetoid spread. The tumor was well differentiated and consisted of germinative, transitional and sebaceous cells. Mitosis and mild and moderate pleomorphism were observed. Ultrastructural findings revealed lipid droplets in the tumor cells although Sudan III staining failed to show any positive materials. 相似文献
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M.L. Jensen 《Journal of cutaneous pathology》1990,17(2):117-121
Extraocular sebaceous gland carcinomas of the skin are uncommon neoplasms that may recur locally, but in contrast to their ocular counterparts infrequently metastasize. A case is reported in which a 62-year-old woman had a 1 cm scalp tumor incompletely excised. Microscopic examination revealed a sebaceous carcinoma. No further surgical treatment was performed and 31 months after diagnosis the patient presented with regional and distant metastases resulting in death. It is emphasized that extraocular sebaceous carcinoma may behave in a biologically aggressive manner, just as their counterparts arising in the ocular adnexae, and the necessity to ensure complete tumor excision is stressed. 相似文献
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【摘要】 患者男,67岁,因头顶部皮损1年余来院就诊。体检:头顶部一淡红色环形斑块,约1.5 cm × 1cm,中央凹陷,边缘见淡黄色丘疹样突起,表面无毛发生长。皮损组织病理检查:表皮轻度增生,表面部分区域凹陷,真皮内见多个皮脂腺融合增生;真皮浅层见较多条索状嗜碱性上皮细胞及角囊肿,周围胶原纤维明显增生。免疫组化结果:CD34阳性(毛源性间质),上皮膜抗原、细胞角蛋白20阳性,bcl?2、P53、CD56、Ⅳ型胶原纤维均阴性,增殖指数Ki67 2% ~ 5%。病理诊断:结缔组织增生性毛发上皮瘤伴皮脂腺增生。 相似文献
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Panfolliculoma with an endophytic architecture resembling a hair follicle: a report of three cases 下载免费PDF全文
Vitaly Terushkin Shane Meehan Ladan Shahabi Nooshin Brinster 《Journal of cutaneous pathology》2016,43(11):1074-1076
Panfolliculoma is a benign follicular tumor comprised of all components of the hair follicle. We report three cases of panfolliculoma with a solid, endophytic architecture, which at scanning magnification had the profile of a hair follicle. The epithelial components included uniform dark blue germinative cells, matrical cells, clear cells and cells containing trichohyaline granules. All the cases also had a central hyperkeratotic horn resembling a hair shaft. Two patients were female and one was male. Two lesions were located on the head and neck, and one was located on the leg. Clinical differential diagnoses included basal cell carcinoma, foreign body and cyst. 相似文献
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报告1例皮脂腺痣合并毛母细胞瘤。患者男,39岁。左面部皮疹30余年,无自觉症状。皮肤专科情况:左面部见一个4 cm× 2 cm大小的皮色斑块,表面粗糙。斑块基础上可见两个约黄豆大小、表面光滑的蓝灰色半球形肿物和一个黄豆大小的乳头状淡红色肿物,质中。浅表淋巴结未触及肿大。皮肤镜下可见蓝灰色均质结构、分枝状血管、黄白色叶状结构。皮损组织病理示:真皮浅层内可见大量皮脂腺、由基底样细胞构成的上皮性肿瘤,伴色素沉着,肿瘤间质纤维组织增生,基底样细胞具有毛囊特征。免疫组化示AR(-), Ki-67(15%+), BCL-2(+),CD10(灶性+),CD34(-),CK20(散在+),Ber-EP4(+)。结合临床表现及病理检查,诊断为皮脂腺痣合并毛母细胞瘤。手术完整切除皮损,随访半年无复发。 相似文献
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<正>临床资料患者,男,14岁。因额部起蜡样斑块十余年,于2018年8月至武汉市第一医院皮肤科就诊。患者出生后即发现其额部一淡黄色斑块,表面蜡样光泽,不伴明显自觉症状,随年龄增长逐渐增大增厚,未予治疗。两月前于搔抓后,斑块中间起一绿豆大淡褐色丘疹,无破溃,无明显自觉症状。既往体健。体格检查:一般情况良好。皮肤科检查:额部正中可见一3.0 cm×2.5 cm大淡黄色斑块,境界尚清,斑块上可见一直径为0.5 cm淡褐色丘疹,表面尚光滑,质韧 相似文献
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患者女,18岁.因头顶部脱发斑18年,破溃结痂14年就诊.患者出生时头顶偏左侧即有甲盖大脱发斑,随其成长皮损缓慢增大,呈淡黄色,逐渐高出皮面,表面粗糙不平,局部无毛发生长.14年前增生斑块的枕后部出现破溃,有黏液性分泌物.患者13岁时皮损生长较快,梳发时破溃处经常有分泌物流出,并结痂,一直未愈合.曾在当地医院诊断为脂溢性皮炎、斑秃等,外用多种糖皮质激素制剂治疗,无明显疗效,于2007年11月21日来我院就诊.继往史、家族史、个人史均无特殊. 相似文献
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Hidradenoma papilliferum is a benign tumor that usually occurs in the female anogenital region. We present a 52-year-old male with a non-anogenital (ectopic) hidradenoma papilliferum on his face. He had had a subcutaneous tumor on his right eyebrow for 30 years. The histological findings included variously shaped cystic and tubular structures in the tumor. The lumina were surrounded by a double layer of cells and showed active decapitation secretion. The lesion contained sebaceous differentiation, which has not been previously documented in the histopathology of hidradenoma papilliferum. We review the published work of non-anogenital (ectopic) hidradenoma papilliferum tumors on the head and neck. 相似文献