1.Cowden Disease Associated with Lhermitte-Duclos Disease: A Case Report.
Bo Ram PARK ; Eui Jong KIM ; Woo Suk CHOI
Journal of the Korean Radiological Society 2006;55(4):327-331
Cowden's disease (CD) is rare multiple hamartoma-neoplasia syndrome. Lhermitte-Duclos disease (LDD) is well known to be a hamartoma of the cerebellum. CD may be accompanied with LDD and other multiple systemic neoplasias. We report here on a case of CD-LDD complex with multiple systemic neoplasia.
Brain
;
Cerebellum
;
Hamartoma
;
Hamartoma Syndrome, Multiple*
2.Eccrine Angiomatous Hamartoma Treated by Intense Pulsed Light.
Tae Gwang KWON ; Hyun HWANGBO ; Young Seok LEE ; Sook Kyung LEE
Korean Journal of Dermatology 2014;52(2):136-137
No abstract available.
Hamartoma*
3.A clinical study of pulmonary hamartoma.
Sung Eun KIM ; Hong Lyeol LEE ; Se Kyu KIM ; Joon CHANG ; Chul Min AHN ; Sung Kyu KIM ; Won Young LEE ; Kyu Ok CHOE ; Kyung Young CHUNG ; Dong Hwan SHIN
Tuberculosis and Respiratory Diseases 1993;40(5):565-574
No abstract available.
Hamartoma*
4.A case of multiple endobronchial hamartomas.
Sung Kyu PARK ; Kyoung Joo RHEE ; Mee Ja PARK ; Sun Young KIM
Tuberculosis and Respiratory Diseases 1992;39(1):83-88
No abstract available.
Hamartoma*
5.Fibrous Hamartoma of Infancy: Report of three cases.
Eun Hee SUH ; Kyung Ja CHO ; Geung Hwan AHN ; Je Geun CHI
Korean Journal of Pathology 1985;19(2):202-206
Fibrous hamartoma of infancy is a distinct clinicopathologic entity with unique microscopic findings and benign clinical course. This tumor is composed of intervening dense fibrocollagenous trabeculae, well defined mucoid areas and varying amounts of mature fat, which are arranged in organoid growth pattern. We report three typical cases of this tumor which were experienced during the recent two years at the Seoul National University Hospital. It is the first description on this tumor in Korean literature. Case 1 was a 10 month old boy who was admitted due to a mass in the right infra clavicular area for 6 months. The mass showed irregular and poorly circumscribed outer surface. Case 2 was a one month old girl who was presented with a diffuse ill defined hairy mass in the left buttock since birth. Case 3 was a 15 month old boy who was brought to the hospital due to well circumscribed scrotal mass fot 8 months. Microscopically all three cases showed very similar histological features. And all 3 cases are well after the removal of the tumors.
Hamartoma
6.Segmentally Arranged Hyperpigmented Basaloid Follicular Hamartoma.
Tae Hyung KIM ; Seung Joon OH ; You Chan KIM ; Mi Ryung ROH
Annals of Dermatology 2015;27(2):218-220
No abstract available.
Hamartoma*
7.A Case of Late Stage Sebaceous Trichofolliculoma Showing Overlapping Features with Folliculosebaceous Cystic Hamartoma.
Eun Jae SHIN ; Ki Heon JEONG ; Min Kyung SHIN
Annals of Dermatology 2016;28(4):511-512
No abstract available.
Hamartoma*
8.Intrapulmonary hamartoma: 2 case report.
Hyung Joon KIM ; Woo Sang CHUNG ; Young Hak KIM ; Jung Ho KANG ; Haeng Ok JEE
The Korean Journal of Thoracic and Cardiovascular Surgery 1992;25(6):577-580
No abstract available.
Hamartoma*
9.A Case of Eccrine-Pilar Angiomatous Hamartoma Showing an Unusual Clinical Manifestation.
Kyu Han KIM ; Hyang Joon PARK ; Yoo Shin LEE
Korean Journal of Dermatology 1984;22(5):549-552
No abstract available.
Hamartoma*
10.A Case of Congenital Neurofollicular Hamartoma.
Yun Seon CHOE ; Jung Yoon OHN ; Kyu Han KIM
Korean Journal of Dermatology 2016;54(2):153-154
No abstract available.
Hamartoma*
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