ABSTRACT
Genital rejuvenation requires medical and procedural treatments that can improve the morphology or aesthetics of the scrotum and vagina. Angiokeratomas are benign vascular lesions that my occur on the penis, scrotum, and vulva. These lesions can be of either cosmetic concern or medical significance if they bleed. Laser therapy can be successfully utilized for the treatment of genital angiokeratomas in men and women.
Subject(s)
Angiokeratoma , Genital Diseases, Male , Laser Therapy , Skin Neoplasms , Vulvar Diseases , Angiokeratoma/therapy , Female , Genital Diseases, Male/therapy , Humans , Male , Rejuvenation , Scrotum/pathology , Vulva , Vulvar Diseases/therapyABSTRACT
BACKGROUND: We present an adolescent with multiple vulvar angiokeratomas within a background of lichen sclerosus. CASE: A 13-year-old girl presented with vulvar pruritus and wart-like vulvar lesions. Four lesions were resected because of discomfort and uncertainty of the diagnosis. Pathology revealed angiokeratomas with chronic inflammation suggestive of lichen sclerosus. Postoperatively, pruritus continued in the largest excised lesion, which was associated with lichen sclerosus, and symptoms were treated successfully with topical steroids. SUMMARY AND CONCLUSION: Vulvar angiokeratomas are asymptomatic red papular lesions and are rare in the female adolescent population. In this case, the pathology revealed the rare co-occurrence of angiokeratomas and lichen sclerosus. Biopsies of vulvar vascular lesions in symptomatic adolescents are recommended. Vulvar angiokeratomas might manifest rare genetic disease in otherwise asymptomatic female patients and warrant further follow-up.
Subject(s)
Angiokeratoma/diagnosis , Skin Neoplasms/diagnosis , Vulvar Lichen Sclerosus/diagnosis , Administration, Topical , Adolescent , Angiokeratoma/pathology , Angiokeratoma/therapy , Female , Humans , Skin Neoplasms/pathology , Skin Neoplasms/therapy , Steroids/administration & dosage , Vulva/pathology , Vulvar Lichen Sclerosus/pathology , Vulvar Lichen Sclerosus/therapyABSTRACT
A 9 year old male presented with diffuse swelling on his tongue since childhood associated with intermittent bleeding. On examination there was multiple, sessile, firm, pinkish, erythematous, shiny papules on both dorsal and ventral surface of the tongue. Angiokeratomas are vascular malformations of capillaries characterized clinically by asymptomatic, solitary or multiple, keratotic papules or plaques, and histologically by benign vascular ectasia of the papillary dermis. Treatment usually consists of local excision and intralesional injection of steroids.
Subject(s)
Angiokeratoma/diagnosis , Skin Neoplasms/diagnosis , Angiokeratoma/therapy , Child , Hemorrhage , Humans , Hypertension , Male , Skin Neoplasms/therapy , Tongue/pathology , Vascular MalformationsABSTRACT
Introduction : L'angiokeratome est une lesion cutanee rare pouvant se presenter soit sous forme d'une lesion solitaire; soit sous forme de papules multiples associees a des troubles metaboliques et rentrants dans le cadre d'une atteinte systemique generalisee. L'atteinte de la cavite orale est plus frequente dans la forme systemique et la localisation linguale est extremement rare. Observation : Les auteurs rapportent une nouvelle observation d'angiokeratome solitaire linguale chez un patient age de 37 ans qui s'est presente pour une masse linguale nodulaire bien limitee douloureuse et saignante au contacte sans particularite. L'examen dermatologique n'a pas retrouve de lesions cutanees associees. Une biopsie exerese a conclu a un angiokeratome. L'evolution etait bonne; sans recidive avec un recul de 1 an. A partir de cette observation et une revue de la litterature; sont discutes les aspects epidemiologiques; cliniques; histologiques et therapeutiques de cette entite extremement rare. Conclusion : L'angiokeratome de la langue est rare; face a ce diagnostic; un examen general minutieux est indispensable pour eliminer une maladie systemique
Subject(s)
Angiokeratoma/diagnosis , Angiokeratoma/epidemiology , Angiokeratoma/therapy , TongueSubject(s)
Angiokeratoma/therapy , Intense Pulsed Light Therapy , Skin Neoplasms/therapy , Aged , Humans , Male , ScrotumABSTRACT
Anderson-Fabry disease is an X-linked lysosomal storage disorder caused by a defect in the α-galactosidase A gene, which leads to the deficiency of the hydrolytic enzyme α-galactosidase A. The consequent inability to catabolize glycosphingolipids causes progressive accumulation of globotriaosylceramide in the vascular endothelium throughout the body. Fatalities in the classical phenotype may usually occur as a consequence of cerebral, cardiac or renal disease. Dermatological manifestations are a relevant feature of Fabry disease and include angiokeratomas, telangiectasiae, lymphedema, anhidrosis or hypohidrosis and pseudo-acromegalic facial appearance. The actual causal treatment for Fabry disease is the enzyme replacement therapy. Dermatologists have a key role, since cutaneous manifestations may lead to the diagnosis. This may help an early therapeutic intervention, reducing both morbidity and mortality.
Subject(s)
Angiokeratoma/etiology , Fabry Disease/complications , Skin Neoplasms/etiology , alpha-Galactosidase/metabolism , Age Factors , Angiokeratoma/diagnosis , Angiokeratoma/metabolism , Angiokeratoma/therapy , Diagnosis, Differential , Enzyme Replacement Therapy , Fabry Disease/diagnosis , Fabry Disease/metabolism , Fabry Disease/therapy , Female , Humans , Male , Sex Characteristics , Skin/blood supply , Skin/enzymology , Skin/pathology , Skin Neoplasms/diagnosis , Skin Neoplasms/metabolism , Skin Neoplasms/therapy , alpha-Galactosidase/administration & dosage , alpha-Galactosidase/therapeutic useABSTRACT
BACKGROUND: Angiokeratomas are papular telangiectasias having a common histology of ectasia of the superficial dermal vessels surmounted by a hyperkeratotic epidermis. PATIENTS AND METHODS: The patient was a 9-year-old girl born of non-consanguineous parents after a well-followed pregnancy with problem-free delivery at term. From birth, she had a tumefaction of the left side of the nose and the left half of the upper lip that gradually increased in size without obstructing the nasal orifice and bled easily. Examination revealed the presence of tumefaction of the left nostril and the left half of the upper lip projecting towards the contralateral side especially in the nose. It was soft and painless, with the presence at the surface of dull red keratotic papules of 1 to 2 mm in diameter. Examination of the nasal mucosa revealed the same appearance of papules. DISCUSSION: Angiokeratoma circumscriptum is a rare congenital malformation, the rarest of five types. Since its initial description in 1890, few cases have been reported. However, female predominance has been noted with a male/female sex ratio of 1/3. It appears to be due to a genetic mutation that is probably autosomal, but the site of which is still unknown. In view of the special features of this case, several diagnoses were suggested, including Rendu Osler's disease, superficial lymphangioma and verrucous angioma. CONCLUSION: The particularity of this case is that it includes the first description of this site, which posed a therapeutic problem, especially concerning the choice of laser type to be used.
Subject(s)
Angiokeratoma/diagnosis , Lip Neoplasms/diagnosis , Nose Neoplasms/diagnosis , Skin Neoplasms/diagnosis , Angiokeratoma/genetics , Angiokeratoma/pathology , Angiokeratoma/therapy , Biopsy , Child , Diagnosis, Differential , Female , Humans , Laser Therapy , Lip Neoplasms/genetics , Lip Neoplasms/pathology , Lip Neoplasms/therapy , Nose Neoplasms/genetics , Nose Neoplasms/pathology , Nose Neoplasms/therapy , Skin/pathology , Skin Neoplasms/genetics , Skin Neoplasms/pathology , Skin Neoplasms/therapyABSTRACT
Indian skin with its broad range of skin color and complexion differs in the presentation and management of cutaneous vascular lesions. Common congenital and acquired vascular lesions are discussed with respect to the epidemiology, clinical presentation, and management strategies in an Indian setting. An effort has been made to review Indian case reports and studies of cutaneous vascular lesions, potential possible modification in the conventional treatment considering resource constraints, cultural practices, availability and cost-effectiveness of the laser and light sources, camouflage techniques, and sclerotherapy. The review concludes with emphasis on the need of availability of cost-effective, quality equipment customized to Indian skin and quality studies and trials for the management of cutaneous vascular lesions in an Indian setting.
Subject(s)
Hemangioma/diagnosis , Hemangioma/therapy , Skin Diseases/diagnosis , Skin Diseases/therapy , Skin Neoplasms/diagnosis , Skin Neoplasms/therapy , Angiokeratoma/therapy , Cosmetics/therapeutic use , Granuloma, Pyogenic/pathology , Granuloma, Pyogenic/therapy , HIV Infections/complications , Hemangioma/pathology , Humans , India , Klippel-Trenaunay-Weber Syndrome/diagnosis , Laser Therapy , Lymphangiectasis/therapy , Port-Wine Stain/complications , Port-Wine Stain/pathology , Port-Wine Stain/therapy , Sarcoma, Kaposi/drug therapy , Sarcoma, Kaposi/virology , Sclerotherapy , Skin Diseases/pathology , Skin Neoplasms/pathology , Sturge-Weber Syndrome/diagnosis , Telangiectasis/therapyABSTRACT
Angiokeratomas are benign tumors characterized by ectasia of blood vessels in the papillary dermis associated with acanthosis and hyperkeratosis of the epidermis. Dermatological examination of angiokeratomas of Fordyce is characterized by papular keratotic lesions of erythematous-violet color. They are more common in the scrotum, and vulvar involvement is rarely reported. Histopathology is particularly important to distinguish them from other benign and malignant tumors. The article reports the case of a middle-aged black woman with a history of chronic constipation, varicose veins of the lower limbs and cesarean section performed 20 years ago who had had multiple vulvar angiokeratomas for three months.
Subject(s)
Angiokeratoma/diagnosis , Skin Neoplasms/diagnosis , Vulvar Neoplasms/diagnosis , Angiokeratoma/therapy , Female , Humans , Middle Aged , Skin Neoplasms/therapy , Vulvar Neoplasms/therapyABSTRACT
Os angioceratomas são tumores benignos caracterizados por ectasia dos vasos sanguíneos da derme papilar associada à acantose e hiperceratose da epiderme. Ao exame dermatológico, os angioceratomas de Fordyce caracterizam-se por lesões papulo-ceratóticas de coloração eritemato-violácea. São mais comuns no escroto, sendo raramente relatada a localização vulvar. A histopatologia é particularmente importante para difer enciá-los de outros tumores benignos e malignos. O artigo relata o caso de uma mulher negra de meia idade com história de obstipação intestinal, varizes de membros inferiores e cesárea há 20 anos que apresentava múltiplos angioceratomas vulvares há três meses.
Angiokeratomas are benign tumors characterized by ectasia of blood vessels in the papillary dermis associated with acanthosis and hyperkeratosis of the epidermis. Dermatological examination of angiokeratomas of Fordyce is characterized by papular keratotic lesions of erythematous-violet color. They are more common in the scrotum, and vulvar involvement is rarely reported. Histopathology is particularly important to distinguish them from other benign and malignant tumors. The article reports the case of a middle-aged black woman with a history of chronic constipation, varicose veins of the lower limbs and cesarean section performed 20 years ago who had had multiple vulvar angiokeratomas for three months.
Subject(s)
Female , Humans , Middle Aged , Angiokeratoma/diagnosis , Skin Neoplasms/diagnosis , Vulvar Neoplasms/diagnosis , Angiokeratoma/therapy , Skin Neoplasms/therapy , Vulvar Neoplasms/therapyABSTRACT
Los angioqueratomas son lesiones vasculares benignas que histopatológicamente están formadas por vasos capilares dilatados subepidérmicos, asociados a una reacción epidérmica con acantosis e hiperqueratosis. Clínicamente podemos encontrar lesiones solitarias o múltiples, en forma de pápulas o placas de pequeño tamaño de color rojo a negro, en variadas localizaciones y con una superficie hiperqueratósica. Presentamos el caso de un niño de 5 años con un angioqueratoma solitario localizado en el tronco que presenta una dermatoscopia característica (AU)
Angiokeratomas are benign vascular lesions that histopathologically consist of subepidermal dilated capillary vessels, associated to an epidermal reaction with acanthosis or hyperkeratosis. Clinically we can find solitary or multiple lesions, as small size red to black papules or plaques, in several locations with an hyperkeratosis surface. We present the case of a solitary angiokeratoma in a 5-years-old child, located on the trunk, with a characteristic dermatoscopy (AU)
Subject(s)
Humans , Male , Child , Angiokeratoma , Angiokeratoma/complications , Angiokeratoma/diagnosis , Angiokeratoma/epidemiology , Angiokeratoma/etiology , Angiokeratoma/surgery , Angiokeratoma/therapy , Cerebrovascular Trauma , Cerebrovascular Trauma/complications , Vascular NeoplasmsABSTRACT
El angioqueratoma nevoide circunscrito es el más raro de los cinco tipos de angioqueratomas descritos en la literatura. Estas lesiones usualmente están presentes al nacimiento y no se relacionan con enfermedad sistémica. Presentamos el caso de un hombre de 32 años con cuadro clínico de angioqueratoma nevoide circunscrito tratado con crioterapia, con buena respuesta inicial.
Subject(s)
Angiokeratoma/therapy , Cryotherapy , Fabry Disease , ThighABSTRACT
Various laser treatment modalities for angiokeratomas have been reported in the literature. A 60-year-old male patient presented for the treatment of multiple angiokeratomas of the scrotum and a 56-year-old female patient presented for the treatment of vulvar angiokeratomas. A 1064 nm long-pulsed Nd:YAG laser was used to treat the patients' lesions. The patients received two laser treatment sessions at an interval of 2 months. Nd:YAG laser treatment yielded successful results in the treatment of our patients' scrotal and vulvar angiokeratomas following two application sessions. We suggest that a long-pulsed Nd:YAG laser is a safe and effective method for the treatment of angiokeratoma of Fordyce.
Subject(s)
Angiokeratoma/therapy , Genital Diseases, Male/therapy , Laser Therapy , Scrotum/pathology , Vulvar Diseases/therapy , Female , Humans , Male , Middle AgedABSTRACT
Fabry disease (FD) is a rare X-linked lysosomal storage disorder resulting from the deficient activity of the enzyme alpha-galactosidase A. Angiokeratomas (AKs) are a frequent manifestation of this disease. They usually become apparent during childhood and can cause important cosmetic disability. Current treatment of this feature in the setting of FD has been mainly based on the application of laser systems, namely the argon laser, the variable pulse width 532-nm Nd:YAG laser, the 578-nm copper vapor laser and the flashlamp-pumped pulsed dye laser. We report the case of a 31-year-old Caucasian woman with a clinical and molecular (GLA p.R118C) diagnosis of FD, presenting multiple AKs scattered over the buttocks and thighs. She was treated with 10 sessions of intense pulsed light (IPL), with a 4-8-week interval between them. An almost complete clearance of the lesions was obtained, with no scars or significant complaints. No recurrence occurred during a 12-month follow-up period. The IPL source can be considered a suitable, effective and safe treatment modality for these cutaneous lesions that typically affect patients with FD, with no need for local anesthesia and with very satisfactory cosmetic results. To our best knowledge, there are no reports in the literature of Fabry's AKs treated with IPL.
Subject(s)
Angiokeratoma/therapy , Fabry Disease/pathology , Phototherapy/methods , Skin Neoplasms/therapy , Adult , Angiokeratoma/pathology , Buttocks , Female , Humans , Microscopy, Electron , Skin Neoplasms/pathology , ThighABSTRACT
Angiokeratoma is a benign vascular lesion. It is the result of dilation of ectatic subdermal vessels and congested capillaries. Weakness of the vessel walls, either from acquired or congenital reasons, can cause formation of the lesion. Angiokeratoma is more common in males, in whom it forms on the scrotal wall. An equivalent form can occur in females, generally on the vulva. The clitoris is an extremely rare location. We present the case of a 14-year-old girl with a clitoral angiokeratoma. To our knowledge, this is the first presented case of clitoral angiokeratoma in a child in English published reports.
