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Osteonecrosis of the jaw (ONJ) is a rare but serious lesion of the jaw, characterized mainly by exposed necrotic bone;it is related to various drugs, usually used for treating patients with advanced malignancies. Drugs implicated in ONJ are: nitrogen-containing bisphosphonates (NBPs), denosumab, anti-angiogenic drugs (e.g bevacizumab, sunitinib,sorafenib) and the selective mammalian target of rapamycin mTOR, everolimus. Previous data regarding the combining of NBPs with antiangiogenic agents conflict with some reports (indicating a similar risk of ONJ compared with the use of NBPs alone1); other reports show significantly higher rates (18% vs 1% with NBPs alone) of the incidence of ONJ2. The mTOR is a serine/threonine kinase, a component of a complex signaling pathway, involved in cell growth and metabolism, reducing VEGF levels and inhibiting the growth and proliferation of tumor cells, endothelial cells, fibroblasts and blood vassels. Everolimus has been approved for the treatment of advanced breast cancer, neuroendocrine tumors of pancreatic origin (pNET), and advanced renal cell carcinoma (RCC). This case report may help to explain the temporal relationship between therapy and the occurrence of ONJ with the sequential use of NBPs and mTOR. A 64-year-old male patient underwent a left, radical nephrectomy in 1992 for clear-cell renal carcinoma. In July 2010 he developed a bone metastasis and he was treated with zoledronic acid 4 mg IV every 4 weeks between 7 July 2010 and 17 August 2012. In February 2011 he had another recurrence, a lung metastasis treated with lobectomy and everolimus 10 mg/die for 6 months from 11 April 2011 to 31 October 2012. In 13 October 2012 the patient showed a facial enlargement and oral fistula in the first quadrant with no history of tooth extraction. A bone scan revealed an ill-defined radiolucency and an orosinusal communication. In January 2013 the patient underwent a right and partial left maxillectomy and is currently being followed up to minimize the risk of new adverse reactions.

Sebaceous carcinoma (SC) is an uncommon neoplasm. To date fewer than 400 cases have been reported in literature. Due to the low incidence and the not universally accepted histopathological classification, it presents diagnostic problems1. Generally, the lesions arise in the meibomian glands of the eyelid. However, extra-ocular localisation in the head and neck region have been reported. While several reports have documented sebaceous adenomas arising from sebaceous glands of the oral cavity, oral sebaceous carcinomas are extremely rare. To date only six cases have been described2. The salivary glands too are considered an uncommon site, even if some cases arising in the parotid gland were recognised. Herein we reported a case of SC arising in the lateral edge of the lower lip in a 71-year-old men. To the best of our knowledge this is the second case described in lips. The clinical differential diagnosis included squamous cell carcinoma, basal cell carcinoma with sebaceous differentiation (BCCSD) and salivary gland neoplasms. The operation was performed under local anaesthesia. The lesion was removed with 0.5 cm of free margins and a W shaped wedge. The defect was primarily closed. The post-operative course was uneventful. Although SC may be found among the multiple sebaceous neoplasms occurring in association with multiple visceral carcinomas in the Muir-Torre syndrome, in the present case the lip was the only localisation of SC. SC must be distinguished from basal cell carcinoma with sebaceous differentiation (BCCSD). The diagnosis may be facilitated by lipophylic stains on frozen sections or immunostains for EMA and S-100.