Results 191 to 200 of about 26,191 (234)
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Adenoid cystic carcinoma of the trachea
The Laryngoscope, 1998AbstractObjective: Primary tracheal tumors are rare, occurring in 0.2 per 100,000 persons per year. Adenoid cystic carcinoma (ACC) is the second most common histologic type of tracheal malignancy. Its clinical behavior is different from the other tracheal neoplasms and thus should be studied separately. Study Design/Methods: Retrospective review of the
T, Azar, F W, Abdul-Karim, H M, Tucker
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Adenoid Cystic Carcinoma of the Breast
Southern Medical Journal, 1978We have presented a case of adenoid cystic carcinoma of the breast and reviewed the literature, with emphasis on the behavior of this rare neoplasm and the fact that its prognosis appears to be more favorable than that of other more common histologic types of breast cancer.
A, Steinman, M, Pepus, G, McSwain
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Adenoid Cystic Carcinoma of the Maxilla
Archives of Otolaryngology - Head and Neck Surgery, 1974A series of 28 patients with an adenoid cystic carcinoma of the maxilla were treated at the Netherlands Cancer Institute. By observing these patients for a very long period of time, the poor prognosis confirms the findings in the literature. Some doubt is thrown on the applicability of the concept of complete removal of the tumor, particularly in the ...
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Adenoid Cystic Carcinoma of the Breast
Archives of Surgery, 1967ADENOID cystic carcinoma of the breast is a tumor seen by few surgeons. It has been described as a "vanishingly rare tumour." 1 A survey of 2,623 malignant breast tumors provided only four examples. 2 In addition to its rarity, it is a distinct form of carcinoma in that it is slow growing and lymph node metastases rarely occur.
J A, Hayes, V, Brooks
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Ultrastructure of adenoid cystic carcinoma
Cancer, 1970Ultrastructural examinations of adenoid cystic carcinoma (ACC) have revealed that the tumor cells are classified into 2 types, i.e., type A cells (myoepithelial cells) and type B cells (secretory type cells). In ultrastructure, the neoplastic myoepithelial cells are very similar to normal ones of intercalated duct type, and more resistant against ...
M, Hoshino, I, Yamamoto
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Adenoid Cystic Carcinoma of the Mandible
The Journal of the American Dental Association, 1983Primary adenoid cystic carcinoma of the jaws is a rare neoplasm of salivary gland origin with only nine cases having been previously reported. It is characterized by a slow clinical course and insidious growth pattern that frequently results in metastasis or recurrence, or both.
Gingell, J., Siegel, Michael Alan
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Intraoral adenoid cystic carcinoma
The Journal of the American Dental Association, 1979A case report of adenoid cytic carcinoma of the palate is presented. The clinical manifestations, diagnostic criteria, surgical resection, and prosthetic reconstruction of the patient are discussed.
C, Mader, W D, Gay
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Adenoid Cystic Carcinoma of the Breast
American Journal of Clinical Pathology, 1984The clinical, histologic, cytologic, and ultrastructural features of three adenoid cystic carcinomas of the breast are presented. All three neoplasms occurred in postmenopausal women. One patient was treated by wide re-excision of the biopsy site. Two were treated by modified radical mastectomy; no axillary lymph node metastases were found. None of the
C, Zaloudek, Y C, Oertel, J M, Orenstein
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Adenoid cystic carcinoma of the tongue
The Journal of Laryngology & Otology, 2000Malignant tumours of the salivary glands in children are extremely rare. We present here a 12-year-old girl initially diagnosed as pleomorphic adenoma on fine needle aspiration biopsy, and adenoid cystic carcinoma (ACC) after the lesion was excised and examined by histopathology.
Dal, H +5 more
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Adenoid Cystic Carcinoma of the Palate
Acta Oto-Laryngologica, 1968A histological re-classification of 383 tumours primary in the palate showed an adenoid cystic carcinoma in 37 cases. The relative incidence of this type of tumour is considerably higher in the palate than in the submandibular and parotid glands. A distinct difference is present between the prognosis in tumours at these three sites. Thus, the prognosis
C M, Eneroth, L, Hjertman, G, Moberger
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