منابع مشابه
Pedunculated Chorangioma of Placenta - an Extremely Rare Case Report
Pedunculated chorangioma is extremely rare type of chorangioma. To the best of our knowledge, no case has been reported in Indian literature. We report one such rare case in a twenty two year old primi gravida who delivered a full term live female baby by lower section caesarian section (LSCS). Gross examination revealed a nodular mass attached to the placenta by a pedicle. Histopathological ex...
متن کاملChorangioma placentae
Chorangioma of the placenta is a rare tumor with a frequency of about 1%, which usually presents as a solitary nodule or, less frequently, as multiple nodules. It is found on the fetal surface of the placenta or in placental parenchyma. Most chorangiomas are small and possess no clinical significance. On the contrary, clinically significant chorangiomas, greater then 5 cm or multiple, may be as...
متن کاملpedunculated chorangioma of placenta - an extremely rare case report
pedunculated chorangioma is extremely rare type of chorangioma. to the best of our knowledge, no case has been reported in indian literature. we report one such rare case in a twenty two year old primi gravida who delivered a full term live female baby by lower section caesarian section (lscs). gross examination revealed a nodular mass attached to the placenta by a pedicle. histopathological ex...
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Absence of the sternum or asterniais the rarest developmental anomaly of the stern um. A female newborn is presented with asternia and ASD.
متن کاملTrichoadenoma: A case report
Trichoadenoma is a rare skin tumor first described by Nikolowski. There are variable clinical features and tumors have been diagnosed as cysts, basal cell epithelioma and seborrheic keratosis. The microscopic feature mainly consists of numerous cysts surrounded by eosinophilic cells. Trichoadenoma is benign and treatment is by simple excision. We report a case of trichoadenoma on the nose...
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ژورنال
عنوان ژورنال: Journal of Medicine
سال: 2014
ISSN: 2075-5384,1997-9797
DOI: 10.3329/jom.v14i2.19671