Your browser doesn't support javascript.
loading
Clinicopathological features of congenital hemangioma: a study of 40 cases / 中华病理学杂志
Chinese Journal of Pathology ; (12): 202-206, 2022.
Artigo em Chinês | WPRIM | ID: wpr-935505
ABSTRACT

Objective:

To investigate the clinical and pathologic features, diagnosis and differential diagnosis of congenital hemangioma (CH).

Methods:

Forty cases of CH were diagnosed from January 2017 to December 2020 in Henan Provincial People's Hospital. The clinical and pathological and immunohistochemical data were analyzed, with review of literature.

Results:

There were 24 male and 16 female patients. The lesions were located in the head, neck (11 cases), limbs (14 cases), and trunk (15 cases). The clinical manifestations were congenital painless plaques or masses, the larger ones protruded on the skin surface, mostly dusky purple or bright red, with surrounding white halos. Under low magnification, the tumor was lobular and well demarcated, composed of neo-microvascular lumen of different sizes. The vascular endothelial cells were cuboidal or hobnail in appearance, forming stellar drainage vessels within the lobules. Extra-medullary hematopoiesis was seen in one case of rapidly involuting CH; there were different number of tortuous and dilated vascular lumen between the lobular structures, and some non-involuting CH cases were vascular malformations, which were devoid of lobulated structures. Immunohistochemistry showed that endothelial cells were strongly positive for CD31, CD34 and ERG, while D2-40 and GLUT-1 were negative.

Conclusions:

CH is a benign congenital vascular tumor with characteristic lobulated growth and abnormal blood vessels in the stroma. Pathological diagnosis often needs to be differentiated from infantile hemangioma, pyogenic granuloma, kaposiform hemangioendothelioma and vascular malformation.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Sarcoma de Kaposi / Neoplasias Cutâneas / Células Endoteliais / Síndrome de Kasabach-Merritt / Hemangioendotelioma / Hemangioma Limite: Feminino / Humanos / Masculino Idioma: Chinês Revista: Chinese Journal of Pathology Ano de publicação: 2022 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Sarcoma de Kaposi / Neoplasias Cutâneas / Células Endoteliais / Síndrome de Kasabach-Merritt / Hemangioendotelioma / Hemangioma Limite: Feminino / Humanos / Masculino Idioma: Chinês Revista: Chinese Journal of Pathology Ano de publicação: 2022 Tipo de documento: Artigo