Breast angiosarcomas are rare tumors, their diagnosis is difficult and the prognosis is worst. We report the case of radiation-induced breast angiosarcoma. The diagnosis is histological and was only made on the surgical specimen. The treatment was essentially surgical. Through this case as well as a review of the literature, we have made an update on this disease.
Adenoid cystic carcinoma of Bartholin’s gland is a rare tumor. Its management is inspired by the treatment of vulvar cancers. We present here a clinical case of a 28-year-old female patient who presented with a painful swelling of the left labia majora, which was mistaken for simple bartholinitis and treated medically without improvement. A biopsy was then performed, and the histopathological study revealed a cystic adenoid carcinoma of the Bartholin gland. The radiological workup showed a locally advanced left vulvar process, without distant metastasis. Due to the impossibility of surgery, concomitant radiotherapy and chemotherapy were performed, with good improvement. The rarity of this type of vascular cancer makes its diagnosis late, because it is often confused with bartholin gland cyst and bartholinitis. Moreover, its management is still not standardized.
Colloid carcinoma of the breast is a rare histological entity, representing only 1 to 6% of all breast carcinomas. It affects a specific population and is known for its favorable prognosis compared to other breast cancers. Through three clinical cases of colloid carcinoma and a review of the literature, we will try to discuss the main clinical-pathological and evolutionary characteristics of this rare form of breast cancer.
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