scholarly journals Aggressive Angiomyxoa of Vulva: Wide local excision case report

2016 ◽  
Vol 7 (11) ◽  
pp. 552
Author(s):  
Krishna Dattatraya Mandade ◽  
Kulsum Ansar ◽  
Aarti Kulkarni
Keyword(s):  
Case Report ◽  
Local Excision ◽  
Wide Local Excision

scholarly journals Paratesticular Liposarcoma: A Case Report and Review of the Literature

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Haider Alyousef ◽  
Elsawi M. Osman ◽  
Mohamed A. Gomha
Keyword(s):  
Case Report ◽  
Local Excision ◽  
Wide Local Excision ◽  
Histopathological Examination ◽  
Well Differentiated ◽  
The Right ◽  
Paratesticular Liposarcoma ◽  
Paratesticular Mass ◽  
Negative Imaging

Introduction. Liposarcoma is a rare pathological entity. By far it is the most common histological subtype of genitourinary sarcomas in adults. Approximately two hundred cases were reported in the literature. We are hereby presenting a case with a typical clinical scenario of paratesticular liposarcoma.Case report. A 75-year-old gentleman presented with a painless right hemiscrotal swelling that was progressively increasing in size over the last 6 years. Testicular tumour markers were negative. Imaging showed a heterogenous mass with fat component. Subsequently he underwent wide local excision that included the paratesticular mass along with the right testicle and all right inguinal canal contents up to the deep inguinal ring with the sparing of right illioinguinal nerve. Histopathological examination showed a well differentiated liposarcoma of the spermatic cord. He remained recurrence-free so far after 18 months of followup.Conclusion. Radical orchidectomy with wide local excision comprises the cornerstone of treatment of paratesticular liposarcoma. Due to the rarity of the disease there is no definite universal consensus of opinion as regards the role of radiotherapy and chemotherapy.

scholarly journals Basal Cell Carcinoma of the Penis: A Case Report and Review of the Literature

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
R. J. Roewe ◽  
Matthew A. Uhlman ◽  
Nathan A. Bockholt ◽  
Amit Gupta
Keyword(s):  
Case Report ◽  
Basal Cell Carcinoma ◽  
Cell Carcinoma ◽  
Local Excision ◽  
Basal Cell ◽  
Wide Local Excision ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Basal Cell Carcinomas

Basal cell carcinoma of the penis is an extremely rare entity, accounting for less than 0.03% of all basal cell carcinomas. Fortunately, wide local excision of such lesions is generally curative. Fewer than 25 cases have been reported in the literature describing penile basal cell carcinoma. Here we report a case of penile basal cell carcinoma cured with wide local excision.

scholarly journals Wide local excision for anal GIST: A case report and review of literature

2017 ◽  
Vol 30 ◽  
pp. 97-100 ◽  
Author(s):  
Mohamed Azzaza ◽  
Houssem Ammar ◽  
Nihed Abdessayed ◽  
Rahul Gupta ◽  
Mohamed Said Nakhli ◽  
...  
Keyword(s):  
Case Report ◽  
Local Excision ◽  
Wide Local Excision ◽  
Review Of Literature

scholarly journals “Deep” vertical Mohs and closure with a tumor-free flap for dermatofibrosarcoma protuberans: A case report

2019 ◽  
Vol 7 ◽  
pp. 2050313X1984778
Author(s):  
Ann M John ◽  
Gina Francisco ◽  
Radhika Srivastava ◽  
Hamza Bhatti ◽  
Babar K Rao
Keyword(s):  
Case Report ◽  
Local Recurrence ◽  
Surgical Technique ◽  
Local Excision ◽  
Free Flap ◽  
Malignant Tumor ◽  
Wide Local Excision ◽  
Dermatofibrosarcoma Protuberans ◽  
High Rate ◽  
Low Grade

Dermatofibrosarcoma protuberans is an uncommon low-grade malignant tumor that can invade locally and rarely metastasize. Dermatofibrosarcoma protuberans has a high rate of local recurrence due to incomplete excision, especially in deep tissues. Morbidity is often related to multiple local recurrences and removal of excessive tissue with large, complex repairs. We present a case of incompletely excised dermatofibrosarcoma protuberans after initial wide local excision. We subsequently employed a “deep” vertical Mohs micrographic surgical technique to remove the remaining tumor while creating a flap with the tumor-free superficial portion to preserve tissue and avoid a complicated repair. The patient is tumor-free for 7 years.

Cutaneous Angiosarcoma of the Scalp Masquerading as a Squamous Cell Carcinoma: Case Report and Literature Review

2012 ◽  
Vol 16 (3) ◽  
pp. 187-190 ◽  
Author(s):  
Padmanabhan Dhanasekar ◽  
Vilvapathy Senguttuvan Karthikeyan ◽  
Nagarajan Rajkumar ◽  
Sarath Chandra Sistla ◽  
S. Manwar Ali ◽  
...  
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Cell Carcinoma ◽  
Local Excision ◽  
Squamous Cell ◽  
Wide Local Excision ◽  
Kaposi Sarcoma ◽  
Neck Region ◽  
The Elderly ◽  
Elderly Male

Background: Cutaneous angiosarcoma is a rare tumor of the elderly male, most commonly affecting the head and neck region. It is difficult to differentiate this tumor from hemangiomas, hemangioblastomas, Kaposi sarcoma, squamous cell carcinoma and anaplastic melanomas. Methods: Case report and review of pertinent English medical literature. Case summary: We report a case of a 60-year-old male presenting with multiple nodules over the scalp where a preoperative histopathologic diagnosis of squamous cell carcinoma was made by wedge biopsy from the tumor. Postoperative histopathology and immuno histochemistry of the wide local excision specimen proved the tumor to be cutaneous angiosarcoma and the patient completed adjuvant radiotherapy. He is now on regular follow-up for 1 year without recurrence. Conclusions: Cutaneous angiosarcoma must be kept in mind in view of its rarity especially in extensive involvement of the scalp by malignancy. The primary treatment is wide local excision with adequate skin cover and adjuvant chemotherapy and radiotherapy in positive margins and lymph node metastasis.

scholarly journals Lymphoepithelioma-Like Carcinoma of the Skin Treated with Wide Local Excision and Chemoradiation Therapy: A Case Report and Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Theresa M. Gille ◽  
Edward F. Miles ◽  
Allen O. Mitchell
Keyword(s):  
Case Report ◽  
Nasopharyngeal Carcinoma ◽  
Local Excision ◽  
Wide Local Excision ◽  
Perineural Invasion ◽  
Chemoradiation Therapy ◽  
Regional Recurrence ◽  
Review Of The Literature ◽  
Positive Margins ◽  
Undifferentiated Nasopharyngeal Carcinoma

Lymphoepithelioma-like carcinoma of the skin (LELCS) is a rare cutaneous neoplasm microscopically similar to undifferentiated nasopharyngeal carcinoma. It is typically nonaggressive and is treated with wide local excision. However, we present a case of a patient with a regional recurrence and more aggressive LELCS with perineural invasion and positive margins for which he was treated with wide local excision followed by chemoradiation. We discuss the use of chemoradiation for this patient and review the literature, specifically pertaining to treatment of more aggressive cases of LELCS.

A RARE CASE OF PRIMARY SQUAMOUS CELL CARCINOMA AT ILEOSTOMY SITE: CASE REPORT

2021 ◽  
pp. 58-59
Author(s):  
Hitesh Soni ◽  
Saurabh Kalia ◽  
J M Mehta ◽  
Manisha Agarwal
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Cell Carcinoma ◽  
Local Excision ◽  
Squamous Cell ◽  
Wide Local Excision ◽  
En Bloc Resection ◽  
Bloc Resection ◽  
Primary Squamous Cell Carcinoma ◽  
En Bloc

Primary squamous cell carcinoma at ileostomy site is extremely rare and there are only eight reported cases prior to our report. The present case report describes a patient of ileostomy formation 12 years prior to evaluation after total colectomy who now presented with mass at stomal and parastomal site and underwent biopsy and Positron emission tomography (PET) scan. Tumor was suspected and hence wide local excision with en bloc resection of the ileostomy and ileo-rectal anastomosis was done and histopathology showed differentiated Squamous cell carcinoma (SCC), Grade 1. This case underlines the need of regular follow-up of patients with stomas to allow the timely detection of stomal problems and the early diagnosis and management of the rare complication of parastomal squamous-cell carcinoma. Also, persistent peristomal ulcerations and proliferative lesions must undergo biopsies to rule out malignancy. Wide local excision of the carcinoma with en bloc resection of ileostomy and formation of new ileostomy at a different site is usually done to manage such cases.

scholarly journals Solitary metastasis of myxoid liposarcoma from the thigh to intraperitoneum: a case report

2019 ◽  
Vol 17 (1) ◽  
Author(s):  
Dong-Wook Kim ◽  
Ye Seob Jee
Keyword(s):  
Case Report ◽  
Local Excision ◽  
Wide Local Excision ◽  
Radical Surgery ◽  
Myxoid Liposarcoma ◽  
Cystic Mass ◽  
Abdominal Tumor ◽  
Case Presentation ◽  
Solitary Metastasis ◽  
Enhanced Computed Tomography

Abstract Background The purpose of case report was to present a rare case of a solitary metastasis of myxoid liposarcoma and discuss the clinical and pathological information for patients treated for metastatic myxoid liposarcoma. Case presentation We report our experience with a case of solitary metastasis of myxoid liposarcoma from the thigh to intraperitoneum. The patient was a 60-year-old man who was referred for abdominal discomfort and fatigue. Enhanced computed tomography showed a 25-cm intra-abdominal tumor. He had undergone a wide local excision for a right thigh myxoid liposarcoma 6 years earlier. At laparotomy, a huge multi-lobular cystic mass was identified at the small bowel mesentery. Wide local excision was performed, and the mass was diagnosed as metastatic myxoid liposarcoma. He was discharged without postoperative complications. Conclusions We experienced a single intraperitoneal metastasis in a patient with myxoid liposarcoma after radical surgery of the primary site.

scholarly journals Anterior mandibular ameloblastoma

2012 ◽  
Vol 2 (1) ◽  
pp. 30 ◽  
Author(s):  
Ajay H. Bhandarwar ◽  
Girish D. Bakhshi ◽  
Ashok D. Borisa ◽  
Amol Wagh ◽  
Rajat Kapoor ◽  
...  
Keyword(s):  
Case Report ◽  
Recurrence Rate ◽  
Local Excision ◽  
Wide Local Excision ◽  
Surgical Excision ◽  
High Recurrence Rate ◽  
Review Of Literature ◽  
Immediate Reconstruction ◽  
Large Size ◽  
Mandibular Region

Ameloblastoma is a benign odontogenic tumor. These are usually asymptomatic until a large size is attained. Ameloblastoma has tendency to spread locally and has a high recurrence rate. Majority of ameloblastomas (80%) arise from the mandible. Ameloblastoma arising from anterior mandibular region (symphysis- menti) is rare. Very few cases of midline anterior ameloblastomas are reported in the literature. They often require wide local excision. Reconstruction of mandible in these cases is challenging. We present a case of mandibular ameloblastoma arising from symphysis- menti. Patient underwent wide surgical excision of the tumor followed by immediate reconstruction using free fibular vascular flap, stabilized with titanium reconstructive plates. A brief case report ands review of literature is presented.

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