Publications by authors named "C Dastamani"

Purpose: To present series of patients with large rare primary lesions of the adrenal glands that were operated in our department. The initial indication for surgery was decided based on their impressive similarity to other more sinister adrenal pathologies.

Methods: The clinical records of the department and histopathology reports, covering the 1986-2015 period were assessed.

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Article Synopsis
  • - Breast myofibroblastomas (MFBs) are rare, benign tumors most frequently occurring in males, often alongside gynecomastia, and definitive diagnosis typically requires post-surgical analysis utilizing immunohistochemistry due to their various tumor variants.
  • - Histologically, MFBs are characterized by spindle cells in a collagenous background, with low mitotic activity and markers such as vimentin and CD34 indicating their benign nature.
  • - Surgical excision, whether through local resection or mastectomy in specific cases, is essential for both diagnosis and treatment, as demonstrated by a study reviewing three instances of MFB, involving two postmenopausal females and one male.
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Introduction: Mucinous cystadenoma is the most common of benign neoplasms of the appendix and carcinoid is the most common type of primary malignant lesions of the appendix.We report a rare case of a 57-year-old female with combined mucinous cystadenoma and carcinoid tumor of the appendix.Dual carcinoid and epithelial neoplasia is a rare occurrence in the appendix.

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Introduction. A peritoneal inclusion cyst is a very rare mesenteric cyst of mesothelial origin usually asymptomatic. A rare case of an 82-year-old white Caucasian female with a femoral hernia containing a large peritoneal inclusion cyst, mimicking strangulated hernia, is presented herein.

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The case of a 20-year-old pregnant woman with a history of one previous cesarean section (CS) who developed a tumorous mass in the area of the CS scar is presented. The clinical diagnosis of endometriosis or fibromatosis was made but the histologic findings were confusing and the pathological diagnosis of an inflammatory type of liposarcoma was made. The case was referred to our Laboratory for re-evaluation and the diagnosis of gossypiboma was made based on histopathological features, the patient's age, her medical history and the exact location of the lesion.

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