Abuawad Yasmin Gama, Diniz Ticiana de Andrade Castelo Branco, Kakizaki Priscila, Valente Neusa Yuriko Sakai
Department of Dermatology, Hospital do Servidor Público Estadual de São Paulo, São Paulo, SP, Brazil.
Department of Dermatology, Hospital do Servidor Público Estadual de São Paulo, São Paulo, SP, Brazil.
An Bras Dermatol. 2020 May-Jun;95(3):347-350. doi: 10.1016/j.abd.2019.04.016. Epub 2020 Mar 19.
Intravascular histiocytosis is a rare condition characterized by the aggregate of histiocytes within dilated dermal vessels. The diagnosis is mainly histophatological and immunohistochemical. We describe a case of a 55 year-old female patient presenting erythematous/purple patches on the breasts, back and limbs. She previously presented ductal carcinoma in the right breast in 2006 which was treated with mastectomy and proceeded to silicone breast implant in 2009. Clinical hypothesis was telangiectatic metastatic carcinoma. Histopathology showed vascular ectasia, thrombosis and recanalization of upper dermis small vessels. On immunohistochemistry, intravascular cells were CD 68+ and negative for estrogen and progesterone receptors, CK7, EMA and AE1/AE3 and endothelial cells were CD64+, leading to the diagnosis of intravascular histiocytosis.
血管内组织细胞增多症是一种罕见病症,其特征为扩张的真皮血管内存在组织细胞聚集。诊断主要依靠组织病理学和免疫组织化学检查。我们报告一例55岁女性患者,其乳房、背部和四肢出现红斑/紫色斑块。她曾于2006年患右乳导管癌,接受了乳房切除术,并于2009年进行了硅胶乳房植入。临床初步诊断为毛细血管扩张性转移性癌。组织病理学显示真皮上部小血管扩张、血栓形成及再通。免疫组织化学检查显示,血管内细胞CD 68阳性,雌激素和孕激素受体、CK7、EMA及AE1/AE3阴性,内皮细胞CD64阳性,最终诊断为血管内组织细胞增多症。