Moderately differentiated neuroendocrine carcinoma (atypical carcinoid) of the larynx.

A moderately differentiated neuroendocrine carcinoma or atypical carcinoid of the larynx occurred in a 68-year-old woman who developed rapidly progressive dysphagia, hoarseness and a neck mass. Immunohistochemical and electron microscopic studies verified the nature of this tumor. Local invasion and distant metastases are common. It is suggested that cigarette smoking could increase the risk of developing this neoplasm.

Primary ovarian carcinoid: a mixture of insular, trabecular and mucinous components.

A case of primary ovarian carcinoid in a 53-year-old woman is described. The tumor which replaced the left ovary showed a mixture of insular, trabecular and mucinous cell types in the same mass. The nature of the neoplastic cells has been verified by light and electron microscopic studies. The latter investigation demonstrated bundles of tonofilament and apical villi of the trabecular cells in addition to the morphologic difference of neurosecretory granules among these various cells.

Mucin-producing malignant meningioma with papillary and glandular patterns.

An exceedingly rare intracranial malignant meningioma with papillary and glandular patterns in a 45-year-old man is described. Intracellular mucin production was demonstrated. The nature of the neoplastic cells was verified by immunohistochemical and electron microscopic studies.

Calcified cystic pituitary prolactinoma.

An unusual cystic pituitary prolactinoma in a 20-year-old man is described. The tumor was roentgenographically calcified. Ultrastructurally, the calcium deposits were found within the cytoplasm of tumor cells, extracellular spaces and blood vessels. The mechanism of intratumoral calcification is discussed in relation to degeneration of neoplastic cells and reparative process.

Lipoblastic meningioma: a light and electron microscopic study.

A patient with intracranial lipoblastic meningioma in the right frontal lobe is reported. The tumor was entirely made up of vacuolated cells. The nature of this rare neoplasm has been verified by light and electron microscopic studies.

Adenosquamous carcinoma of the thyroid: a case report and review of the literature.

A case of mixed squamous cell carcinoma and papillary adenocarcinoma of the thyroid in a 75-year-old woman is described. Review of 19 reported adenosquamous carcinoma including the present case revealed that they tended to occur in the sixth and seventh decades of life with an average age of 63.84 years and without sexual predilection. Local invasion and metastases of this highly fatal neoplasm are common.

Congenital hemihypertrophy with adrenocortical adenoma.

A rare case of adrenocortical adenoma in a 7-month-old female infant with congenital hemihypertrophy of left leg is described. Only 7 similar cases including the present one, are on record. The patients ranged in age from 7 weeks to 45 years. The male:female ratio was 3:4. The adrenal tumors were often detected after CH had become evident. Large functional tumors often produced symptoms of hirsutism, virilization, and precocious puberty. CT and ultrasound are necessary for early detection and prompt treatment.