ABSTRACT
Schwannoma is a benign nerve sheath tumour rarely found in the head and neck region and much less commonly found in the intraparotid facial nerve. It is a slow-growing encapsulated tumour arising from differentiated Schwann cells or axonal nerve sheath. It can occur anywhere along the course of the facial nerve. Patients most commonly present with an asymptomatic swelling, in the absence of any signs of facial nerve palsy. Accordingly, diagnosis is usually difficult before surgical removal and histopathological examination. Here, we report a rare case of facial nerve schwannoma (FNS), diagnosed on fine needle aspiration cytology, in a 35-year-old male who presented with a painless, gradually increasing swelling in the right infra-auricular region for the last 2 years. His general examination revealed no signs of facial muscle weakness. The cytodiagnosis of intraparotid FNS was further confirmed by immunohistochemistry on cell block.
Subject(s)
Cranial Nerve Neoplasms , Facial Nerve Diseases , Facial Paralysis , Neurilemmoma , Adult , Biopsy, Fine-Needle , Cranial Nerve Neoplasms/diagnosis , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/surgery , Facial Nerve/pathology , Facial Nerve Diseases/diagnosis , Facial Paralysis/pathology , Humans , Male , Neurilemmoma/diagnosis , Neurilemmoma/pathology , Neurilemmoma/surgery , Parotid Gland/pathologyABSTRACT
Objective: Endometrial cancer (EC) is the most commonly diagnosed malignancy and has the second-highest mortality rate among gynecological cancers. Adenomyosis is well-known for abnormal uterine bleeding and is a widely reported entity; however, an EC arising from the adenomyosis is a rare event; even rarer is the occurrence of serous endometrial carcinoma. Case report : A 60-year post-menopausal female presented with post-menopausal bleeding. Subsequently, she underwent a hysterectomy, which showed atrophic and cystic endometrium with extensive adenomyosis and atypical endometrial glands, which are diffusely P53 positive with intervening negative benign and focally positive dysplastic endometrial glands. A final diagnosis of serous endometrial carcinoma arising from adenomyosis was rendered. In a table format, previously reported serous endometrial carcinoma Arising cases from adenomyosis using PubMed search had been described. Conclusion: Serous endometrial carcinoma arising from adenomyosis (<20 cases reported) and has a slightly more dismal prognosis than those deriving from the endometrial cavity. Hence, this case report highlights the occurrence, rarity, and importance of such an entity.
ABSTRACT
Pure yolk sac tumor is the most frequently seen testicular tumor in childhood; however it is usually a component of mixed germ cell tumor in adults. Pure yolk sac tumors are quite rare in adults. Pure yolk sac tumor in adults has been categorized as yolk sac tumor, post-pubertal type. We report a case of pure yolk sac tumor of right testis with lung metastasis in a 37-year-old man who was successfully treated by high inguinal orchidectomy and BEP combination chemotherapy.
