K
Kenneth O. Devaney
Researcher at University of Michigan
Publications - 170
Citations - 7951
Kenneth O. Devaney is an academic researcher from University of Michigan. The author has contributed to research in topics: Carcinoma & Neck dissection. The author has an hindex of 48, co-authored 170 publications receiving 7249 citations. Previous affiliations of Kenneth O. Devaney include University of Rochester & Henry Ford Allegiance Health.
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Journal ArticleDOI
Neuroendocrine neoplasms of the larynx: advances in identification, understanding, and management.
TL;DR: Laryngeal small cell neuroendocrine carcinomas are chiefly treated by way of radiation and chemotherapy; the role of adjuvant therapy in the treatment of atypical carcinoid tumours remains to be established.
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Review of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) of head and neck.
Antonino Carbone,Alberto Passannante,Annunziata Gloghini,Kenneth O. Devaney,Alessandra Rinaldo,Alfio Ferlito +5 more
TL;DR: The entity known as sinus histiocytosis with massive lymphadenopathy (SHML), or Rosai-Dorfman disease, is an uncommon benign proliferation of hematopoietic and fibrous tissue that often presents in the head and neck region.
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Squamous cell carcinoma of the buccal mucosa
Scott E. Strome,Scott E. Strome,Wyatt C. To,Myla Strawderman,Myla Strawderman,Kevin Gersten,Kevin Gersten,Kenneth O. Devaney,Kenneth O. Devaney,Carol R. Bradford,Carol R. Bradford,Ramon M. Esclamado,Ramon M. Esclamado +12 more
TL;DR: It is concluded that wide local excision for early-stage buccal carcinoma is associated with a high local failure rate and possible causes for failure and alternative treatment approaches are discussed.
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Pediatric Myofibromatosis of the Head and Neck
TL;DR: Myofibromatosis is a distinct disorder among the great number of fibrous proliferations occurring in infants and children, with a particular predilection for the head and neck region, and many of these lesions show spontaneous regression, suggesting that lesions not affecting vital functions, resulting in growth anomalies, or demonstrating rapid aggressive growth may be managed conservatively.
Journal ArticleDOI
Parathyroid carcinoma: a review.
Randall P. Owen,Carl E. Silver,Phillip K. Pellitteri,Ashok R. Shaha,Kenneth O. Devaney,Jochen A. Werner,Alessandra Rinaldo,Alfio Ferlito +7 more
TL;DR: Parathyroid carcinoma is a rare entity, comprising fewer than 1% of cases of hyperparathyroidism and occasionally with vocal cord paralysis or a firm palpable cervical mass.