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1.
Article in English | MEDLINE | ID: mdl-24439916

ABSTRACT

OBJECTIVE: Apigenin and kaempferol are plant flavonoids with reported chemopreventive activities. This study aimed to determine the effect of apigenin and kaempferol on cell viability in cultured cells derived from the pharynx (FaDu cell line), an oral cavity carcinoma (PCI-13 cell line), and a metastatic lymph node (PCI-15B cell line) and in explanted FaDu cells. STUDY DESIGN: The in vitro viability of FaDu, PCI-13, and PCI-15B cells treated with apigenin and kaempferol was determined. Tumor growth of FaDu explants was evaluated in athymic mice that were gavaged with either apigenin or kaempferol. RESULTS: Although apigenin and kaempferol treatment decreased viability of cells in vitro, cell-type-dependent differences in responsiveness were observed. In vivo apigenin treatment significantly increased the tumor size of FaDu explants. Results obtained using kaempferol were similar. CONCLUSIONS: The in vitro decrease in FaDu cell viability by apigenin and kaempferol was not observed in in vivo tumor explants using the conditions described in this study.


Subject(s)
Apigenin/pharmacology , Head and Neck Neoplasms/drug therapy , Kaempferols/pharmacology , Animals , Cell Line, Tumor , Cell Survival/drug effects , Female , Humans , Mice , Mice, Nude
2.
Otolaryngol Head Neck Surg ; 149(4): 541-6, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23894148

ABSTRACT

OBJECTIVE: While the success of microvascular reconstruction is well established, even in the setting of prior radiotherapy, the outcomes in the setting of prior chemoradiation are less well documented. We present our experience with microvascular reconstruction in a unique cohort of patients previously treated with concomitant hyperfractionated radiation and intra-arterial chemotherapy (HYPERRADPLAT). Despite the observation in prior studies of minimal vessel damage in this setting, the hypothesis of this study is that in the late setting of most salvage surgical therapy, either for recurrence or osteoradionecrosis, a different, progressive level of vessel injury may be encountered. STUDY DESIGN: Case series with chart review. SETTING: Tertiary referral academic medical center practice. SUBJECTS AND METHODS: Eighty-four patients received primary treatment for advanced head and neck squamous cell carcinoma with HYPERRADPLAT. Of these, 8 patients (10%) underwent free tissue transfer reconstruction and a total of 11 free flaps. RESULTS: Wound breakdown, fistula, or both occurred postoperatively in 50% (4/8) of these patients. No complications of the venous anastomoses occurred. Fifty percent (4/8) of patients required return to surgery for arterial failure due to thrombosis of the anastomosis. Two cases of these flaps could not be salvaged. CONCLUSION: Microvascular reconstruction following HYPERRADPLAT appears to result in a high number of arterial related complications. This experience implies an important delayed treatment effect of HYPERRADPLAT occurs upon recipient arteries. The manner in which this effect may occur in recipient arteries in the setting of more conventional chemoradiation requires further study.


Subject(s)
Carcinoma, Squamous Cell/therapy , Free Tissue Flaps , Head and Neck Neoplasms/therapy , Adult , Antineoplastic Agents/administration & dosage , Chemoradiotherapy , Cisplatin/administration & dosage , Dose Fractionation, Radiation , Female , Free Tissue Flaps/adverse effects , Humans , Injections, Intra-Arterial , Male , Middle Aged , Neoplasm Recurrence, Local/surgery , Squamous Cell Carcinoma of Head and Neck , Treatment Outcome
3.
Ear Nose Throat J ; 90(3): E8-E10, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21412733

ABSTRACT

Spontaneous perforation of the esophagus is an uncommon event; when it does occur, it usually affects the thoracic esophagus. We present a rare and fatal case of spontaneous perforation of the cervical esophagus in a 68-year-old woman. We believe this rupture was related to a proximal outlet obstruction secondary to cricopharyngeal muscle dysfunction.


Subject(s)
Esophageal Perforation/diagnosis , Esophageal Perforation/etiology , Pharyngeal Muscles/physiopathology , Aged , Esophageal Perforation/therapy , Female , Humans
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