Abstract:Melanomas of the skin are poorly circumscribed lesions, very frequently asymptomatic but unfortunately with a continuous growing incidence. In this landscape, one can distinguish melanomas originating in the mucous membranes and located in areas not exposed to the sun, namely the vulvo-vaginal melanomas. By contrast with cutaneous melanomas, the incidence of these types of melanomas is constant, being diagnosed in females in their late sixties. While hairy skin and glabrous skin melanomas of the vulva account … Show more
“…In general, the female gender appears to be a risk factor for MM, as they are twice as common in women compared to men. In contrast, cutaneous melanoma (CM) distribution is similar between both genders [ 4 ] . Additionally, certain genetic alterations are found to be associated with MM: activating mutations in SF3B1 and KIT, loss of CDKN2A, PTEN or SPRED1, and amplification of CDK4, TERT, KIT, MDM2 or CCND1.…”
Section: Discussionmentioning
confidence: 99%
“…Gene sequencing of MM helps identify driver mutations and provides therapeutic opportunities for targeted therapy. The most common presenting complaint of vaginal melanomas is genital bleeding, while others include a palpable mass, itching, dyspareunia, yellow genital secretions, and local pain [ 4 ] . The diagnosis of vaginal melanomas includes pathological analysis and IHC of the biopsy sample, imaging to determine extent, and genetic testing.…”
Section: Discussionmentioning
confidence: 99%
“…IHC can be helpful in difficult cases to confirm that the neoplasm is of melanocytic origin. Widely used markers include protein S-100, melanoma antigen recognized by T-cells-1 (MART-1) or Melan-A, melanoma-specific antigen (HMB-45), microphthalmia transcription factor (MITF), and vimentin [ 4 ] . Due to the lack of an adequate number of cases to conduct randomized clinical trials, prognostic factors and treatment protocols are not clearly defined for vaginal melanoma.…”
Introduction: Primary vaginal malignant melanomas are rare tumours with a limited number of cases published in the literature. They primarily affect post-menopausal women with a median age of 57–68 years and have a dismal prognosis. The 5-year survival rate, regardless of treatment, is approximately 5–25%. Case description: We present the case of an 87-year-old female who presented with haematuria and urinary incontinence. She was diagnosed with AJCC stage IIIC vaginal melanoma. Considering her age and the extent of malignancy, surgery was not a viable option and immunotherapy with nivolumab and ipilimumab was initiated as treatment. Discussion: The diagnosis of vaginal melanomas includes pathological analysis and immunohistochemistry (IHC) of the mass, imaging to determine extent, and genetic testing. Surgery is the preferred treatment in suitable cases. For metastatic or unresectable cases, immunotherapy or targeted therapy is the preferred first-line treatment. Due to the lack of an adequate number of cases to conduct randomized clinical trials, prognostic factors and treatment protocols for vaginal melanomas are not clearly defined. At present, the management of these tumours is largely based on retrospective studies and anecdotal evidence accompanied by significant knowledge gaps. Our case will be a valuable addition to the existing literature on vaginal melanomas that are managed non-surgically.
“…In general, the female gender appears to be a risk factor for MM, as they are twice as common in women compared to men. In contrast, cutaneous melanoma (CM) distribution is similar between both genders [ 4 ] . Additionally, certain genetic alterations are found to be associated with MM: activating mutations in SF3B1 and KIT, loss of CDKN2A, PTEN or SPRED1, and amplification of CDK4, TERT, KIT, MDM2 or CCND1.…”
Section: Discussionmentioning
confidence: 99%
“…Gene sequencing of MM helps identify driver mutations and provides therapeutic opportunities for targeted therapy. The most common presenting complaint of vaginal melanomas is genital bleeding, while others include a palpable mass, itching, dyspareunia, yellow genital secretions, and local pain [ 4 ] . The diagnosis of vaginal melanomas includes pathological analysis and IHC of the biopsy sample, imaging to determine extent, and genetic testing.…”
Section: Discussionmentioning
confidence: 99%
“…IHC can be helpful in difficult cases to confirm that the neoplasm is of melanocytic origin. Widely used markers include protein S-100, melanoma antigen recognized by T-cells-1 (MART-1) or Melan-A, melanoma-specific antigen (HMB-45), microphthalmia transcription factor (MITF), and vimentin [ 4 ] . Due to the lack of an adequate number of cases to conduct randomized clinical trials, prognostic factors and treatment protocols are not clearly defined for vaginal melanoma.…”
Introduction: Primary vaginal malignant melanomas are rare tumours with a limited number of cases published in the literature. They primarily affect post-menopausal women with a median age of 57–68 years and have a dismal prognosis. The 5-year survival rate, regardless of treatment, is approximately 5–25%. Case description: We present the case of an 87-year-old female who presented with haematuria and urinary incontinence. She was diagnosed with AJCC stage IIIC vaginal melanoma. Considering her age and the extent of malignancy, surgery was not a viable option and immunotherapy with nivolumab and ipilimumab was initiated as treatment. Discussion: The diagnosis of vaginal melanomas includes pathological analysis and immunohistochemistry (IHC) of the mass, imaging to determine extent, and genetic testing. Surgery is the preferred treatment in suitable cases. For metastatic or unresectable cases, immunotherapy or targeted therapy is the preferred first-line treatment. Due to the lack of an adequate number of cases to conduct randomized clinical trials, prognostic factors and treatment protocols for vaginal melanomas are not clearly defined. At present, the management of these tumours is largely based on retrospective studies and anecdotal evidence accompanied by significant knowledge gaps. Our case will be a valuable addition to the existing literature on vaginal melanomas that are managed non-surgically.
“…Treatment specialty-specific characteristics and outcomes in women with vulvo-vaginal melanoma: A JGOG-JSCS joint study Melanoma of the female genitalia, including the vulva and vagina, represents a rare type of malignancy that is associated with poor survival outcomes. [1][2][3] Due to the rarity, vulvo-vaginal melanomas have been relatively understudied and treatment often includes overlap between the dermatologists, representing expertise in melanoma, and the gynecologists who possess the expertise in female genital tract malignancy.…”
mentioning
confidence: 99%
“…While various studies have reported prognostic factors for vulvovaginal melanomas, [1][2][3][4][5] the prognostic effect of treating specialty for vulvo-vaginal melanomas (dermatologists vs. gynecologists) has not been previously examined. The objective of the current study was to compare characteristics and outcomes of women with vulvo-vaginal melanoma based on the specialty of the physician guiding treatment.…”
Infectious etiologies have previously been proposed as causes of both melanoma and non‐melanoma skin cancer. This exploratory overview explains and presents the evidence for the hypothesis that a microorganism excreted in infected ruminant animal feces, Mycobacterium avium subspecies paratuberculosis (MAP), is the cause of some cases of cutaneous melanoma (CM). Occupational, residential, and recreational contact with MAP‐contaminated feces, soil, sand, and natural bodies of water may confer a higher rate of CM. Included in our hypothesis are possible reasons for the differing rates and locations of CM in persons with white versus nonwhite skin, why CM develops underneath nails and in vulvar skin, why canine melanoma is an excellent model for human melanoma, and why the Bacille Calmette‐Guérin (BCG) vaccine has demonstrated efficacy in the prevention and treatment of CM. The pathogenic mechanisms and etiologic aspects of MAP, as a transmittable agent underlying CM risk, are carefully deliberated in this paper. Imbalances in gut and skin bacteria, genetic risk factors, and vaccine prevention/therapy are also discussed, while acknowledging that the evidence for a causal association between MAP exposure and CM remains circumstantial.
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