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This variation in pattern further emphasizes the need to sample tumors adequately generalized anxiety symptoms dsm 5 order 25 mg tofranil with mastercard. Morphologically highgrade tumors are composed predominantly of solid tumor with a paucity of distinct vascular channels. In these tumors distinction from other spindle cell neoplasms is the main problem. Conservative surgery with radiotherapy is increasingly used in the treatment of breast cancer, and it is estimated that about 0. The interval between radiation exposure and develop ment of angiosarcoma is usually between 2 and 10 years. Angiosarcoma arising after radiotherapy is more common than de novo angiosar coma, and, because it is associated with breast cancer treatment, it is seen in older women. Atypical vascular lesions can also arise after radiotherapy and must be dis tinguished from welldifferentiated angiosarcoma. The tumor has a very aggressive behavior, spreading rapidly through the area of lymphedema and disseminating widely throughout the body. Histologically the tumor is composed of papillary or solid growth of poorly differentiated spindle cell or epithelioid cells. This morphology led to speculation that these tumors may represent retrograde vascular spread of breast carcinoma cells rather than true angiosarcoma. Immunohistologic and ultrastructural studies, however, confirmed that they are vascular in origin769,770 and best regarded as veryhighgrade lymphangiosarcoma. An invasive pure spindle cell tumor with a mesenchymal phenotype (vimentin positivity only). Clin ically the tumor presents with a short history of a mass, which on examination is firm and freely mobile. These lesions are rounded and well circumscribed and have a vague multinodular cut surface appearance. These tumors are circumscribed and have a false capsule of compressed breast tissue, with only rare entrapped mammary parenchymal structures. They are composed of spindle cells often arranged in short bundles within a collagenous stroma. The nuclei are oval or stubby with slightly irregular outline, small nucleoli, and occasional grooves. Ultrastructurally the tumor cells contain bundles of myofilaments with focal densities. Other Sarcomas Most types of sarcoma have been described at least rarely in the breast.

However anxiety symptoms vs panic attacks buy tofranil 25 mg line, they have the potential to invade adjacent organs and metastasize to hilar lymph nodes. Germ Cell Tumors Teratomas, both benign and malignant, can originate within the lung in rare instances. They can present with cough, hemoptysis, and chest pain and occasionally with the expectoration of hair. Their histopathologic features are identical to those of teratomas arising in the gonads (see Chapter 14). Some authors believe that all such cases actually represent unusual carcinoid tumors, because normal paraganglia have not been demonstrated in the lung. The tumors are characterized by a proliferation of round to oval cells with large, often hyperchromatic nuclei with stippled chromatin and abundant amphophilic cytoplasm. The tumor cells often adopt a nested (Zellballen) pattern of growth typical of neuroendocrine neoplasms. Rosettes, ribbons, trabeculae, or festoons are not a feature of paragangliomas and serve to differentiate them from bronchial carcinoids. Another distinguishing feature that helps to separate these tumors from carcinoid is the presence of marked nucleomegaly with occasionally multilobated and hyperchromatic nuclei. Another distinctive feature is the presence of a network of S-100 protein­positive sustentacular cells surrounding the nests of tumor cells, although such cells have also been described in carcinoid tumors. The majority of cases are benign and treated adequately by surgical resection alone. Granular Cell Tumor of Bronchus Granular cell tumor of bronchus is an unusual lesion in the lung. The presence of extrapulmonary granular cell tumors in association with such a lung tumor has been described. Marked cellular atypia, necrosis, hemorrhage, and mitotic activity are not generally seen. The overlying bronchial epithelium can show squamous metaplasia, but no evidence of invasion by tumor cells will be seen. Ganglioneuroblastoma Ganglioneuroblastoma is an exceedingly rare tumor of lung (see Chapter 28). At least in one case, the tumor was associated with the multiple endocrine neoplasia syndrome, but this finding may have been coincidental. Grossly, the tumors are well circumscribed and can measure up to 5 cm in diameter.

True papillary adenocarcinoma of the lung is believed to exhibit considerably worse morbidity and mortality than bronchioloalveolar carcinoma anxiety kids buy tofranil 50 mg mastercard. A "micropapillary" variant of pulmonary adenocarcinoma has also been described characterized by small, abortive micropapillary structures reminiscent of similar tumors arising in the breast and bladder. B, Poorly differentiated squamous carcinoma with central comedo-like areas of necrosis. Sections taken from the junction between apparently normal bronchial mucosa and frank squamous cell carcinoma will often display changes that range from squamous metaplasia to intraepithelial atypia (dysplasia) to carcinoma in situ. Occasional lesions may show prominent clearing of the cytoplasm due to accumulation of glycogen. In the past, such tumors were referred to as clear cell carcinomas of the lung and were identified as a separate category. Squamous cell carcinoma with prominent clear cell change, however, will behave in the same manner as conventional squamous cell carcinoma; it therefore does not warrant classification as a separate type. Three other rare histologic variants, however, deserve mention (see following discussion). Spindle Cell Squamous Carcinoma Spindle cell squamous carcinoma, also known as sarcomatoid carcinoma, is a tumor characterized by an appearance that mimics sarcoma. However, focally, the tumor cells are usually seen to blend with areas of more conventional squamous cell carcinoma. The most important distinction is with spindle cell sarcoma, although some cases of sarcomatoid carcinoma may have a prominent chronic inflammatory component and simulate inflammatory pseudotumor. Grading of squamous cell carcinoma into well, moderately, and poorly differentiated types will depend on the degree of squamous differentiation within the tumor, such as the presence of intercellular bridges and keratinization. Well-differentiated tumors are characterized by sheets of cells that adopt a pavement-like architecture and contain ample eosinophilic cytoplasm, round to oval nuclei, and prominent nucleoli. In the less differentiated tumors, the above features may be observed only focally, and the lesions are characterized by more pronounced cytologic atypia, increased mitotic activity, and frequent areas of necrosis and/or hemorrhage. A central, comedo-type pattern of necrosis is typically seen in the higher grade lesions. The latter probably represents a more poorly differentiated variant of the same tumor with more pronounced cytologic atypia and pleomorphism, multinucleated tumor cells, and correspondingly more aggressive behavior. Lymphoepithelioma-like Carcinoma Lymphoepithelioma-like carcinoma61,62 corresponds to a poorly differentiated squamous carcinoma with prominent lymphoid stroma, similar to those occurring in the nasopharynx. The tumor cells are characterized by large, vesicular nuclei with prominent eosinophilic nucleoli surrounded by a scant rim of cytoplasm. The tumor cell islands are characteristically surrounded by a prominent lymphoplasmacytic host response. The main histologic component of this tumor appears to be the spindle cell component, which is usually admixed in various proportions with a highly pleomorphic malignant giant cell component. In some cases, focal areas of conventional adenocarcinoma or squamous cell carcinoma may be present, and, as such, some authors prefer to regard these lesions as a phenotype rather than as an entity. The older designation of "undifferentiated large cell carcinoma" should be abandoned because the epithelial nature of the neoplasm has been amply demonstrated by immunohistochemical and ultrastructural studies; hence, a more accurate designation would be poorly differentiated anaplastic carcinoma rather than undifferentiated.

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