Charanjeet Ahluwalia

Diagnosis of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) by fine needle aspiration cytology

Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma. Hence, it is important to distinguish Rosai–Dorfman disease from lymphoma and other causes of histiocytosis because of the different treatment modalities. We report here a case of Rosai–Dorfman presenting with massive bilateral cervical lymphadenopathy. We conclude that fine needle aspiration cytology is a useful and reliable tool for the diagnosis of Rosai-Dorfman disease due to which biopsy can be avoided in these patients, thus, reducing inconvenience to patients.

Aggressive angiomyxoma of vulva in a 13-year-old female.

Aggressive angiomyxoma is a rare mesenchymal neoplasm that typically affects females of reproductive age. It involves preferentially pelvic and perineal regions and was first described by Steeper and Rosai in 1983. Peak age of incidence for this tumor is in the fourth decade with very few cases reported in young girls. We present a case of this rare tumor in a 13-year-old female.

Primary non-Hodgkin's lymphoma of the female genital tract in a 27-year-old female: A rare case report

Primary non-Hodgkins lymphoma (NHL) of the female genital tract is a rare tumor mainly affecting the elderly age group. A preoperative diagnosis is difficult to reach due to varied clinical presentation and lack of diagnostic features on radiological investigations. We present an unusual case of primary NHL affecting uterus, cervix, and bilateral ovaries in a 27-year-old female.