An Exceptional Vulvar Tumor

2020 ◽  
Vol 39 (2) ◽  
pp. 111-114
Author(s):  
Karishma P. Ramlakhan ◽  
Floris H. Groenendijk ◽  
Mark-David Levin ◽  
Leonard A. Noorduyn ◽  
Sjarlot G. Kooi
Keyword(s):  
Vulvar Tumor

scholarly journals SCALED CELL CARCINOMA TYPE VERRUCOUS INFILTRATED – CASE STUDY

2019 ◽  
Vol 7 (4) ◽  
pp. 11-16
Author(s):  
Dr. Xavier Antonio Chan Gómez ◽  
Dr. Jorge Daher Nader ◽  
Bella Vallejo López
Keyword(s):  
Squamous Cell Carcinoma ◽  
Cell Carcinoma ◽  
Squamous Cell ◽  
Histopathological Diagnosis ◽  
Early Complications ◽  
Early Health ◽  
Vulvar Tumor ◽  
Present Case Study

Disorders in patients who develop squamous cell carcinoma can lead to severe conditions. The present case study evidences the advance of this pathology in a patient who goes to the medical services when the problem has advanced. Objective- To describe the case of a patient who underwent surgery to remove a tumor from the vulvar region to prevent it from triggering in severe states. Method - Surgery of a vulvar tumor, performed on a female patient of 62 years. Result- Squamous cell carcinoma, infiltrative verrucous type, with dimensions of 7x6 cm, with an invasion depth of 2.7 mm in the central region    Conclusion- This type of pathology should not be allowed to worsen when it occurs, as it deteriorates the quality of life of patients over the years. If it is detected and treated early, complications can be avoided. In the present case, the histopathological diagnosis was epidermoid carcinoma. It is expected that the information collected will be useful to professionals and that it contributes as an alert to detect early health problems in patients.

scholarly journals VULVAR TUMOR - CASE REPORT AND LITERATURE REVIEW

2019 ◽  
Vol 2 (2) ◽  
pp. 69-73
Author(s):  
Zimmermmann JB ◽  
de Morais BCF ◽  
de Paula AJF ◽  
Costa ALM ◽  
Dias BA ◽  
...  
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Literature Review ◽  
Epithelial Tumors ◽  
Rare Tumors ◽  
Fibroepithelial Polyps ◽  
Source Tissue ◽  
Vulvar Tumor

The vulvar region is a complex area because it comprises many elements, besides the skin itself. Therefore, it can present a variety of relatively rare tumors that can be classified based on source tissue (epithelial or mesenchymal). Benign epithelial tumors in the connective tissue are not often diagnosed in the vulvar area, which is mostly affected by fibroepithelial polyps.

scholarly journals Cellular Angiofibroma: A Rare Vulvar Tumor Case Report

2020 ◽  
Vol 42 (06) ◽  
pp. 365-368
Author(s):  
Ana Helena Barbosa Fachada ◽  
Cátia Sofia Guilherme Ferreira Pais ◽  
Marta Andrea Ferreira Fernandes ◽  
Nuno Jorge Lopes Dias ◽  
António Manuel Leitão Loureiro Pipa
Keyword(s):  
Case Report ◽  
Preoperative Diagnosis ◽  
Clinical Presentation ◽  
Good Prognosis ◽  
Mesenchymal Tumor ◽  
Cellular Angiofibroma ◽  
Benign Mesenchymal Tumor ◽  
Vulvar Tumor ◽  
Risk Of Relapse

AbstractCellular angiofibroma (CA)is a rare benign mesenchymal tumor. In women, it occurs mainly in the vulvovaginal region, with vulvar location in 70% of the cases. Its clinical presentation is nonspecific and similar to several other vulvar tumors of different cellular origins. Thus, its histological and immunohistochemical features allow distinction from other tumors. Cellular angiofibromas have good prognosis, despite some risk of relapse. The authors present the case of a 49-year-old woman with a bulky right vulvar lesion, for which the preoperative diagnosis was a Bartholin cyst, but the histological and immunohistochemical evaluation yielded a CA.

A multidisciplinary approach to fertility-sparing therapy for a rare vulvar tumor

2010 ◽  
Vol 93 (1) ◽  
pp. 267.e5-267.e7 ◽  
Author(s):  
Cary L. Dicken ◽  
Harry J. Lieman ◽  
Ashlesha K. Dayal ◽  
Subhakar Mutyala ◽  
Mark H. Einstein
Keyword(s):  
Multidisciplinary Approach ◽  
Fertility Sparing ◽  
Vulvar Tumor

scholarly journals Association of a large vulvar tumor in a in a young premenopausal woman with recurrent pseudoangiomatous stromal hyperplasia of the breasts

2020 ◽  
Vol 26 (1) ◽  
pp. 16-18
Author(s):  
Angelica Knickerbocker ◽  
Douglas Timmons ◽  
Youley Tjendra ◽  
Simone Garzon ◽  
Jose Carugno
Keyword(s):  
Surgical Procedures ◽  
Premenopausal Woman ◽  
Breast Tissue ◽  
Reproductive Age ◽  
Pseudoangiomatous Stromal Hyperplasia ◽  
Anogenital Region ◽  
Proliferative Lesion ◽  
Uncommon Condition ◽  
Vulvar Tumor ◽  
Firm Mass

Pseudoangiomatous stromal hyperplasia is a benign proliferative lesion of the breast tissue that typically affects women in the reproductive age. Pseudoangiomatous stromal hyperplasia usually presents as a localized, painless, firm mass or as a diffuse thickened area of the breast. Rarely, it can arise along the embryonic milk line, up to the anogenital region, where it simulates angiosarcomas. Awareness of this uncommon condition is important in order to avoid unnecessary aggressive excisional surgical procedures. For this purpose, we present a case of nodular pseudoangiomatous stromal hyperplasia arising in the vulva in a patient with recurrent pseudoangiomatous stromal hyperplasia of the breast.

Vulvar tumor in children due to prolapse of urethral mucosa

1970 ◽  
Vol 108 (4) ◽  
pp. 572-575 ◽  
Author(s):  
Vincent J. Capraro ◽  
Natalio P. Bayonet-Rivera ◽  
Imre Magoss
Keyword(s):  
Vulvar Tumor

Clinicopathologic Characteristics of 12 Patients With Vulvar Sweat Gland Carcinoma

2010 ◽  
Vol 20 (5) ◽  
pp. 874-878 ◽  
Author(s):  
Jin Lin Hou ◽  
Ling Ying Wu ◽  
Hong Tu Zhang ◽  
Ne Nan Lv ◽  
Ying Huang ◽  
...  
Keyword(s):  
Lymph Nodes ◽  
Tumor Progression ◽  
Sweat Gland ◽  
Surgical Margin ◽  
Primary Treatment ◽  
The Other ◽  
Inguinal Lymph Nodes ◽  
Sweat Gland Carcinoma ◽  
Gland Carcinoma ◽  
Vulvar Tumor

Objectives:The aim of this article was to evaluate the clinical and pathologic characteristics, therapy, and prognostic factors of vulvar sweat gland carcinoma.Materials:Clinical and pathologic data for 12 patients with vulvar sweat gland carcinoma treated at our institution from January 1958 to April 2009 were retrospectively analyzed. Of the 12 cases, 7 cases were vulvar sweat gland carcinoma, 3 cases were vulvar Paget disease with underlying sweat gland adenocarcinoma, 1 case was vulvar apocrine adenocarcinoma, and 1 case was adenoid cystic carcinoma of the vulvar sweat gland. Two patients were treated with simple vulvar tumor excision at other medical institutions without adjuvant therapy. Among the other 10 patients, 6 underwent radical vulvectomy; 3, wide local excision of the vulva; and 1, a simple vulvectomy. For 5 of the 12 patients, bilateral or unilateral inguinal lymph nodes excision and biopsy were performed. For 1 patient with bulky inguinal lymph nodes, only a biopsy was performed, and the patient received radiotherapy after vulvar surgery.Results:A follow-up for 11 patients was conducted until death or April 1, 2009. Five of the 11 patients had recurrences after primary treatment. For 2 of these patients, recurrence was local 6 and 48 months after treatment. For 3 patients, distant metastasis was found 18, 5, and 31 months after surgery at our institution. Five of 11 patients died, 1 of whom died of irrelevant disease and 4 of tumor progression. The total survival periods of the 4 patients who died of tumor progression were 24, 36, 44, and 203 months. The other 6 patients have survived for more than 5 years without local failure. In total, there are 7 patients who have survived for 5 years or more.Conclusions:Vulvar sweat gland carcinoma is a very rare entity. Surgery is the primary treatment modality, and the function of radiotherapy and chemotherapy is uncertain. The vulvar tumor size and inguinal lymph nodes metastasis will influence the prognosis, with pathologic differentiation and surgical margin status being the probable prognostics factors.

The giant vulvar tumor

2018 ◽  
Vol 17 (5) ◽  
pp. 82-84
Author(s):  
A.I. Davydov ◽  
◽  
V.A. Lebedev ◽  
Keyword(s):  
Vulvar Tumor
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