scholarly journals Surgical Management of Benign Tumors of the Proximal Fibula

2021 ◽  
Vol 5 (9) ◽  
Author(s):  
Kyle Huntley ◽  
Waleed Al-Hardan ◽  
Juan Pretell-Mazzini
2020 ◽  
Vol 2020 ◽  
pp. 1-18
Author(s):  
Mohammed AlKindi ◽  
Sundar Ramalingam ◽  
Lujain Abdulmajeed Hakeem ◽  
Manal A. AlSheddi

Salivary gland tumors (SGT) comprise 3% of all head and neck tumors, are mostly benign, and arise frequently in the parotid gland. Pleomorphic adenoma (PA) is the commonest SGT, representing 60-70% of all benign parotid tumors. Clinically, parotid PA presents as irregular, lobulated, asymptomatic, slow-growing preauricular mass, involving both superficial and deep lobes, and could grow to gigantic proportions. Histologically, PA has epithelial and mesenchymal elements in chondromyxoid matrix and is managed surgically. Based on a review of 43 cases reported in English literature since 1995, giant parotid PA is reported as large as 35 cm (diameter) and 7.3 kg (resected weight). Although rare, 10 cases of malignant transformation were reported in the review. Surgical management included extracapsular dissection (ECD), superficial parotidectomy, and total parotidectomy for benign tumors, and adjuvant radiation or chemotherapy for malignant tumors. We further present the case of a 36-year-old healthy male with slow-growing and asymptomatic giant parotid PA, of 4-year duration. The patient presented with firm, lobulated preauricular swelling, provisionally diagnosed as PA based on radiographic and cytological findings. The tumor was resected through ECD, and the patient had uneventful postoperative recovery and a 7-year recurrence-free follow-up period. Histological examination revealed epimyoepithelial proliferation punctuated by chondromyxoid areas, with extensive squamous metaplasia and keratin cysts. To the best of knowledge from indexed literature, giant parotid PA is rarely reported in Saudi Arabia. In addition to its rarity, this case is reported for its benign nature despite atypical histological presentation, successful surgical management without complications, and long-term recurrence-free follow-up. Based on this report, clinicians must be aware of atypical histological presentations associated with PA and plan suitable surgical management and follow-up to avoid morbidity. Nevertheless, attempts must be made to diagnose and manage these lesions at an early stage and before they reach gigantic proportions.


2013 ◽  
Vol 71 (2) ◽  
pp. 410-413 ◽  
Author(s):  
Giovanni Dell'Aversana Orabona ◽  
Paola Bonavolontà ◽  
Giorgio Iaconetta ◽  
Raimondo Forte ◽  
Luigi Califano

Author(s):  
Hosein Faezypour ◽  
Aileen M. Davis ◽  
Anthony M. Griffin ◽  
Robert S. Bell

2015 ◽  
Vol 55 (4) ◽  
pp. 317-327 ◽  
Author(s):  
Toshihiro TAKAMI ◽  
Kentaro NAITO ◽  
Toru YAMAGATA ◽  
Kenji OHATA

2001 ◽  
Vol 30 (3) ◽  
pp. 141-146 ◽  
Author(s):  
Udai S. Kammula ◽  
Joseph F. Buell ◽  
Daniel M. Labow ◽  
J. Michael Millis ◽  
Mitchell C. Posner

1995 ◽  
Vol 53 (5) ◽  
pp. 506-508 ◽  
Author(s):  
Rainer Laskawi ◽  
Maik Ellies ◽  
Christian Arglebe ◽  
Angrit Schott

2021 ◽  
Vol 11 (3) ◽  
pp. 88-94
Author(s):  
Andrei I Gritsiuta

Primary benign tumors of the sternum are an exceedingly rare entity. Surgical techniques regarding intervention for these lesions are not clearly defined in the literature given their scarcity. Operative techniques include en-bloc resection of the tumor, and this has proven to be successful in preventing local recurrence despite benign nature of the lesion. Given the often extensive defect created by the excision, reconstruction is frequently necessary; depending on the size of the defect, either autologous bone grafting or the use of synthetic materials may be indicated. This study serves to present two cases of rare primary benign tumors of the sternum, giant cell tumors and osteoma spongiosum and to summarize the available literature. We present a review of the literature of 17sternal giant cell tumor cases reported so far including our patient and unique case of osteoma spongiosum of the sternum, that discusses their surgical management, as well as reconstructive techniques that provided an excellent clinical result and a lack of recurrence on long term follow-up.


Neurosurgery ◽  
2010 ◽  
Vol 66 (4) ◽  
pp. 833-840 ◽  
Author(s):  
Allan D. Levi ◽  
Andrew L. Ross ◽  
Esteban Cuartas ◽  
Rabah Qadir ◽  
H. Thomas Temple

Abstract OBJECTIVE To determine the clinical presentation and morbidity of the surgical management of peripheral nerve sheath tumors (PNSTs). METHODS We performed a retrospective chart review of surgically treated PNSTs at the University of Miami between 1991 and 2008. RESULTS There were a total of 140 cases, including 87 schwannomas, 34 neurofibromas, and 19 malignant peripheral nerve sheath tumors (MPNSTs). The average age of the total study group was 49.0 years; it was significantly lower for patients with neurofibroma. There was a high correlation between neurofibroma tumors and neurofibromatosis-1. Most patients with benign tumors presented with a painful mass, paresthesias, or numbness without significant weakness. Patients who had previously undergone attempted resections and preoperative biopsy had a significantly increased risk (41%) for developing postoperative neurologic deficits when compared with patients who presented with de novo tumors (15%). Intraoperative monitoring appeared to reduce the risk of postoperative motor deficit, particularly in neurofibromas. Most MPNSTs (>80%) were diagnosed at stage IIB or higher and had a combined mortality rate of 31.6% at 78 months. Tumor size was the best predictor of adverse outcome, as all MPNST mortalities occurred in patients with a tumor size of more than 7 cm. CONCLUSION PNSTs are a heterogeneous group of lesions. Benign tumors respond well to marginal excision, whereas MPNSTs are aggressive sarcomas that require multimodal management. There was a significantly increased risk of postoperative neurologic deficits in patients who had undergone a previous biopsy, and thus tertiary referral without biopsy is recommended when a PNST is suspected.


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