1.Pulmonary lymphangiomyomatosis.
Soo Sang JUNG ; Byeng Ryul PARK ; Jong Su LEE ; Seok Sung YANG
The Korean Journal of Thoracic and Cardiovascular Surgery 1993;26(2):160-163
No abstract available.
Lymphangioleiomyomatosis*
2.Pulmonary lymphangioleiomyomatosis: high-resolution CT findings.
Woo Kyung MOON ; Jung Gi IM ; Man Chung HAN
Journal of the Korean Radiological Society 1991;27(4):543-546
No abstract available.
Lymphangioleiomyomatosis*
3.Pulmonary lymphangioleiomyomatosis: case reports.
Kyung Soo LEE ; Eun Wan CHOI ; Byoung Ho LEE ; Won Kyung BAE ; Yong Hoon KIM ; Chang Jin KIM ; Joong Kee NOH
Journal of the Korean Radiological Society 1991;27(2):240-244
No abstract available.
Lymphangioleiomyomatosis*
4.Lymphangioleiomyomatosis in Korea.
Eun Kyung MO ; Man Pyo JUNG ; Chul Gyu YOO ; Young Whan KIM ; Sung Koo HAN ; Jung Gi IM ; Jeong Wook SEO ; Seung Sook LEE ; Young Soo SHIM ; Keun Youl KIM ; Yong Chol HAN
Tuberculosis and Respiratory Diseases 1993;40(5):519-531
No abstract available.
Korea*
;
Lymphangioleiomyomatosis*
5.Pulmonary lymphangioleiomyomatosis in Pham Ngoc Thach Hospital: a case report
Ho Chi Minh city Medical Association 2003;8(2):104-106
This rare condition was diagnosed in the stage of a history of resection of left renal tumor of angiomyolipoma and recurrant pneumothrax with PCR of positive tuberculosis bacilla, special chest CT scan with thin wall cyst. These female patients are in reproductive age, using consistantly sex hormone. The prognosis is similar with COPD. Early detection and treatment of the case slowers the progression of disease.
Lymphangioleiomyomatosis
;
Lung
;
Disease
6.Two cases of pulmonary lymphangioleiomyomatosis associated with tuberous sclerosis.
Jeong Cheon AHN ; Weon Yong JOH ; Kwang Ho IN ; Kyung Ho KANG ; Se Hwa YOO
Tuberculosis and Respiratory Diseases 1992;39(6):542-547
No abstract available.
Lymphangioleiomyomatosis*
;
Tuberous Sclerosis*
8.A case of lymphangioleiomyomatosis originated in the pelvic cavity.
Jung Mi HAN ; Kyung Hee LEE ; Sung Joo KIM ; Chae Chun RHIM ; Young Han PARK ; Jung Bae KANG ; Sun Young JEON
Journal of Gynecologic Oncology 2008;19(3):195-198
Lymphangioleiomyomatosis is a rare disease that is characterized by proliferation of abnormal smooth muscle-like cells, especially that which occurs in the pulmonary parenchyme. It primarily affects women of child-bearing age. The majority of primary lymphangioleiomyomatosis occurs in the lung, but there are a few reports of extrapulmonary cases. We experienced a rare case of lymphangioleiomyomatosis which originated in the pelvic cavity (in the posterior portion of the uterus), and report with brief review of literatures.
Female
;
Humans
;
Lung
;
Lymphangioleiomyomatosis
;
Pelvis
;
Rare Diseases
;
Uterus
9.Spontaneous Rupture of Renal Angiomyolipoma in a Female Tuberous Sclerosis Patient with Pulmonary Lymphangioleiomyomatosis.
Jong Wook KIM ; Tae Won LEE ; Myung Joon KIM ; Mi Mi OH ; Jae Hyun BAE ; Hong Seok PARK ; Je Jong KIM ; Kang Soo SHIM
Korean Journal of Urology 2007;48(3):344-347
Pulmonary lymphangioleiomyomatosis (LAM) is uncommon debilitating disease, predominantly affecting women of childbearing age. Renal angiomyolipoma (AML) is the most common renal lesion in patients with tuberous sclerosis (TS), but, even without TS, is reported in up to 60% of the patients with LAM, which is frequently diagnosed several years before the LAM itself. However, it is extremely rare for renal AML and pulmonary LAM to simultaneously present in tuberous sclerosis complex. Herein, a case of spontaneous rupture of a renal AML, accompanied by pulmonary LAM, in a reproductive female with TS, managed by selective transcatheter arterial embolization (TAE), is reported.
Angiomyolipoma*
;
Female*
;
Humans
;
Lymphangioleiomyomatosis*
;
Rupture, Spontaneous*
;
Tuberous Sclerosis*
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