RESUMO
Apocrine hidrocystomas (AHC) are uncommon cystic lesions of apocrine glands and are most often solitary. They are usually found in the head and neck region. Multiple AHC have been rarely reported in the literature usually in the eyelids and face. On extensive search of literature, we came across only a single case report of multiple axillary AHC. We report a case of a 31-year-old female who presented with fullness and discomfort in bilateral axillae, so a clinical diagnosis of bilateral accessory breast was made. However on histopathological examination, it turned out to be bilateral multiple AHC associated with apocrine hyperplasia.
Assuntos
Glândulas Apócrinas/patologia , Axila/patologia , Hidrocistoma/diagnóstico , Hidrocistoma/patologia , Hiperplasia/diagnóstico , Hiperplasia/patologia , Adulto , Feminino , Histocitoquímica , Humanos , MicroscopiaAssuntos
Adenoma Pleomorfo/diagnóstico , Adenoma Pleomorfo/patologia , Osso e Ossos/patologia , Neoplasias de Cabeça e Pescoço/diagnóstico , Neoplasias de Cabeça e Pescoço/patologia , Neoplasias Cutâneas/diagnóstico , Neoplasias Cutâneas/patologia , Histocitoquímica , Humanos , Imuno-Histoquímica , Masculino , Microscopia , Proteínas S100/análise , Adulto JovemRESUMO
Breast hamartomas (BH) or Fibroadenolipoma are extremely rare breast lesions. They are benign, focal malformations that resemble a neoplasm in the tissue of its origin. We describe a case of a 48 year old woman with bilateral breast lumps for the past 18 months and 6 months which were gradually increasing in size. FNAC smears revealed only clusters of benign ductal epithelial cells. Lumps were excised and histopathology revealed predominantly stromal smooth muscle bundles (proved by immunohistochemistry) along with scattered intact terminal duct-lobular units, dilated ducts and entrapped islands of mature fibroadipose tissue. A diagnosis of Bilateral Myoid hamartoma of breast was given. To the best of our knowledge till date no case of bilateral MH of breast has been reported in the literature. We report the first case of bilateral MBH highlighting its morpho-immunophenotypic features.