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1.
Case Rep Pathol ; 2012: 305858, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22934213

RESUMO

Malignant adenomyoepithelioma of the breast is a rare tumour with around 30 cases reported in the literature. Metastases associated with these tumours are usually haematogenous. Axillary lymph node metastases are thought to be unusual, and it has been recently suggested that axillary node dissection is not indicated unless clinically palpable. We here present a case of a 63-year-old woman, who developed a malignant adenomyoepithelioma with axillary lymph node metastasis, that included epithelial and myoepithelial elements, in spite of the absence of clinically enlarged nodes. We suggest that histological examination of axillary sentinel node(s) or node sampling may be worthwhile in this condition.

2.
Arch Pathol Lab Med ; 131(6): 974-8, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17550330

RESUMO

Sclerosing angiomatoid nodular transformation (SANT) is a recently recognized nonneoplastic vascular lesion of the spleen with fewer than 30 cases described. Microscopically, SANT consists of multiple well-circumscribed vascular/angiomatoid nodules showing plump endothelial cell and extravasated erythrocytes. The nodules are surrounded by a variable lymphoplasmacytic infiltrate, spindle cells, and collagenous stroma. The vascular nodules display a complex mixture of endothelial phenotypes resembling splenic sinusoids (CD34-/CD31+/CD8+), capillaries (CD34+/ CD31+/CD8-), and small veins (CD34-/CD31+/CD8-). Focal expression of CD68 can also be seen. The differential diagnosis of SANT includes splenic hamartoma, inflammatory myofibroblastic tumor, littoral cell angioma, and hemangioendothelioma. It has been postulated that SANT represents a peculiar hamartomatous transformation of splenic red pulp in response to an exaggerated nonneoplastic stromal proliferation. SANT has a benign clinical course with splenectomy being curative.


Assuntos
Angiomatose/patologia , Baço/patologia , Esplenopatias/patologia , Angiomatose/metabolismo , Antígenos CD/metabolismo , Biomarcadores/metabolismo , Diagnóstico Diferencial , Feminino , Hamartoma/diagnóstico , Hemangioendotelioma/diagnóstico , Hemangioma/diagnóstico , Humanos , Pessoa de Meia-Idade , Miofibroma/diagnóstico , Baço/metabolismo , Baço/cirurgia , Esplenopatias/metabolismo , Esplenopatias/cirurgia , Resultado do Tratamento
3.
Eur J Dermatol ; 16(5): 576-8, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17101482

RESUMO

We report the case of a 67-year-old woman who presented with a peri-anal skin tag. Histologically, the excised lesion showed features of tubulopapillary apocrine hidradenoma, with an area showing features of carcinoma in situ. The lesion also had papillary and cribriform growth patterns, reminiscent of breast lesions. Similar to vulvar lesions, peri-anal apocrine tumours are believed to arise in mammary like glands (MLGs). To the best of our knowledge, this is the first description of a peri-anal adenocarcinoma in situ arising in a tubulopapillary apocrine hidradenoma. The relationship to MLGs is also discussed.


Assuntos
Adenocarcinoma/patologia , Adenoma de Glândula Sudorípara/patologia , Neoplasias do Ânus/patologia , Carcinoma in Situ/patologia , Neoplasias das Glândulas Sudoríparas/patologia , Idoso , Feminino , Humanos
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