1.Linear angiokeratoma circumscriptum associated with hemangiectatic hypertrophy.
Min Seok SONG ; Yoo Deuk LEE ; Soo Il CHUN
Korean Journal of Dermatology 1991;29(4):544-548
No abstract available.
Angiokeratoma*
;
Hypertrophy*
2.A Case of Angiokeratoma Corporis Diffusum.
Sung Woo CHOI ; Chun Wook PARK ; Eun Hee CHOO ; Guk Joo CHOI ; Hyung Ok KIM ; Chung Won KIM ; Kye Yong SONG
Korean Journal of Dermatology 1984;22(5):522-526
No abstract available.
Angiokeratoma*
;
Fabry Disease*
3.A Case of Acral Pseudolymphomatous Angiokeratoma of Children (APACHE)
Ho Jeong SHIN ; Young Jae KIM ; Chong Hyun WON ; Sung Eun CHANG ; Mi Woo LEE ; Jee Ho CHOI ; Woo Jin LEE
Korean Journal of Dermatology 2018;56(1):74-76
No abstract available.
Angiokeratoma
;
Child
;
Humans
4.A Case of Post-Injury Angiokeratoma Circumscriptum of the Chest.
Na Hyun KWON ; Si Yong KIM ; Gyong Moon KIM
Annals of Dermatology 2010;22(1):66-68
Angiokeratomas represent vascular lesions and are histologically characterized by superficial vascular ectasia and overlying acanthosis and/or hyperkeratosis. Angiokeratomas can be classified into five types, with angiokeratoma circumscriptum representing the least common of the five types. Angiokeratoma circumscriptum presents at birth and frequently occurs unilaterally on the leg. Herein, we report a rare case of long term angiokeratoma circumscriptum (twelve years) on the right chest, discovered following the excision of a lipoma from the same area.
Angiokeratoma
;
Dilatation, Pathologic
;
Leg
;
Lipoma
;
Parturition
;
Thorax
5.A Case of Solitary Angiokeratoma of the Oral Tongue Tip.
Sung Jun WON ; Jin Pyeong KIM ; Jung Je PARK ; Seung Hoon WOO
Korean Journal of Otolaryngology - Head and Neck Surgery 2012;55(2):111-113
Angiokeratoma is a rare, cutaneous disorder that typically manifests as multiple lesions and is often associated with a number of metabolic disorders. Although solitary cutaneous forms have been reported, localized lesions within the oral tongue have not been described so far. We report a 16-year-old male with a solitary pigmented lesion of his oral tongue tip. The lesion was a mixture of purple and white in color with a granulomatous appearance. Histopathological examination of the lesion obtained by excisional biopsy showed features consistent with angiokeratoma. We report a case of solitary angiokeratoma of the oral tongue tip and review the clinical and pathologic features of this unusual condition.
Adolescent
;
Angiokeratoma
;
Biopsy
;
Humans
;
Male
;
Tongue
6.A Case of Cutaneous Horn Arising from Angiokeratoma in Infancy.
Tae Yoon KIM ; Kyung Real LEE ; Se Hee KIM ; Dong Hyun KIM ; Moon Soo YOON
Korean Journal of Dermatology 2007;45(9):959-961
Cutaneous horn is a clinical description for a protruding mass of keratin, which may arise from benign and malignant lesions. There have been 21 cases of cutaneous horns reported in Korea: 19 cases in adults, 2 cases in children, and no case in infants. We report the case of an 8-month-old girl who presented with a pea-sized, hyperkeratotic nodule on the dorsum of the right foot. Histopathologic examination confirmed the nodule to be a cutaneous horn arising from an angiokeratoma.
Adult
;
Angiokeratoma*
;
Animals
;
Child
;
Female
;
Foot
;
Horns*
;
Humans
;
Infant
;
Korea
7.A Case of Solitary Papular Angiokeratoma with Transepidermal Elimination.
Sun Ji KIM ; Hyun Jeong PARK ; Jun Young LEE ; Baik Kee CHO
Korean Journal of Dermatology 2008;46(4):544-546
Transepidermal elimination is a well known phenomenon describing cases where foreign materials or altered dermal constituents are removed from dermis through epidermis. The phenomenon of transepidermal elimination may occur as a primary process or as a secondary process. A 36-year-old women presented with three black papules on the ventral side of her right second toe for 1 year. Because of poliomyelitis, the lesion had been irritated repeatedly. The histopathology of the lesion showed solitary papular angiokeratoma with transepidermal elimination. In this case, we postulated that transepidermal elimination of this case could have developed through repetitive physical trauma.
Adult
;
Angiokeratoma
;
Dermis
;
Epidermis
;
Female
;
Humans
;
Poliomyelitis
;
Toes
8.Scrotal leiomyoma presenting as angiokeratoma of fordyce.
Anclote Melanie S ; Espinoza-Thaebtharm Agnes ; Barcelona-Tan Jesusa
Journal of the Philippine Dermatological Society 2005;14(1):62-64
Scrotal Leiomyoma is an extremely rare benign tumor originating from the tunica dartos muscle. It usually presents as a solitary, painless, unilateral, slow growing mass that is occasionally pedunculated. We report a case of a 31-year-old man, presenting clinically with multiple papules resembling Angiokeratoma of Fordyce but with a histopathologic diagnosis of Scrotal Leiomyoma. Scrotal Leiomyoma has not been reported to present clinically in this manner and our report is probably the first of its kind.
Human ; Female ; Adult ; Angiokeratoma ; Leiomyoma ; Muscles ; Scrotum ; Skin Neoplasms
9.A Case of Acral Pseudolymphomatous Angiokeratoma of Children (APACHE).
Ye Won HAN ; Baik Kee CHO ; Jun Young LEE
Korean Journal of Dermatology 2007;45(5):477-480
Acral pseudolymphomatous angiokeratoma of children (APACHE) is a recently recognized, rare clinical entity with only 20 reported cases worldwide. It is characterized by unilateral eruptions of multiple angiomatous papules, mostly on acral areas and mainly in children, although some cases have also been reported with involvement of non-acral areas and occurring in adults. The histopathologic examination revealed diffuse dermal infiltrates of lymphohistiocytes and thick-walled vessels lined with prominent plump endothelial cells. APACHE is a cutaneous pseudolymphoma, rather than a vascular neoplasm, because of distinct histopathologic and immunohistochemical findings. We report a case of a 9-year-old girl who presented with multiple angiomatous papules on her right upper arm. The histopathologic and immunohistochemical findings in our patient were consistent with a diagnosis of APACHE.
Adult
;
Angiokeratoma*
;
APACHE
;
Arm
;
Child*
;
Diagnosis
;
Endothelial Cells
;
Female
;
Humans
;
Pseudolymphoma
;
Vascular Neoplasms
10.Angiokeratoma of the Vulva.
Seong Hun LEE ; Sung Pil YOON ; Sun Young MOON ; Jae Hak YOO ; Joo Heung LEE ; Seung Chul LEE
Korean Journal of Dermatology 1996;34(6):1013-1015
Angiokeratoma of the vulva is a relatively rare, benign condition that usually presents as single or a few isolated papules mainly on the labia majora. It is histologically identical to angiokeratoma of the scrotum. A 50-year-old woman presented with a one year history of nonpruritic lesions on the vulva. Her skin lesions used to bleed vith subtle trauma. Several dark purplish papules, ranging in diameter from 3 to 5mm, were noticed on both labia majora. A biopsy confirmed the diagnosis of angiokeratoma. A simple electrodesiccation of all lesions was performed under local anesthesia. The patient has remained asymptomatic nd without recurrence for the follow-up period of 10 months without any recurrence.
Anesthesia, Local
;
Angiokeratoma*
;
Biopsy
;
Diagnosis
;
Female
;
Follow-Up Studies
;
Humans
;
Middle Aged
;
Recurrence
;
Scrotum
;
Skin
;
Vulva*