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1.
Journal of the Korean Surgical Society ; : 306-309, 2010.
Article Dans Anglais | WPRIM | ID: wpr-224916

Résumé

We present a 50-year-old woman with left adrenal sarcoidosis. She visited our hospital for right upper quadrant discomfort; she was then evaluated for right upper quadrant discomfort. She had no abnormal findings in the laboratory examination, including hormone study, but a mass was detected at left adrenal gland, incidentally. Initially, we thought the mass as nonfunction adrenal adenoma. After she had undergone laparoscopic left adrenalectomy, she was diagnosed with left adrenal sarcoidosis from her histological findings. Adrenal sarcoidosis is a very rare disease. This case provides insight to the experience of left adrenal sarcoidosis.


Sujets)
Femelle , Humains , Adulte d'âge moyen , Adénomes , Glandes surrénales , Surrénalectomie , Maladies rares , Sarcoïdose
2.
Journal of the Korean Surgical Society ; : 127-130, 2009.
Article Dans Coréen | WPRIM | ID: wpr-185596

Résumé

Castleman's disease (CD) is an uncommon lymphoproliferative disorder of unknown origin. There are two histological types: hyaline-vascular type and plasma cell type. CD is usually located in the mediastinum, but may be seen in any site including the neck, axilla, mesentery, and retroperitoneum. A 52-year-old male complained of vague lower abdominal pain. There was no palpable mass and all laboratory data showed nonspecific findings. Abdominal computed tomography scan showed a solitary homogenous, well-defined mass in the mesentery. The laparoscopic complete resection was performed without complications. Histologic examination of resected lesion revealed the hyaline-vascular type of CD. In the hyaline-vascular type of CD, laparoscopic approach constitutes a complete treatment. We present here the case of laparoscopic treatment of isolated mesenteric CD.


Sujets)
Humains , Mâle , Adulte d'âge moyen , Douleur abdominale , Aisselle , Hyperplasie lymphoïde angiofolliculaire , Syndromes lymphoprolifératifs , Médiastin , Mésentère , Cou , Plasmocytes
3.
Journal of the Korean Society for Vascular Surgery ; : 106-112, 2008.
Article Dans Coréen | WPRIM | ID: wpr-77789

Résumé

PURPOSE: Takayasu's arteritis (TA) is a chronic inflammatory, stenotic or aneurysmal disease of an unknown etiology. TA occurs worldwide, but it disproportionately affects young females of Asian descent. TA is known to affect a variety of vessels, but the subclavian artery, axillary artery, carotid arteries and infraabdominal aorta are most frequently affected. In this article, we evaluated surgical treatment as a modality for the management for TA. METHOD: We retrospectively reviewed 20 patients with TA and who were operated on from January 1994 to December 2007. RESULT: The ages of patients were ranged from 12 to 56 years. The ratio of males to females was 1 to 19. The main affected vessels were the subclavian artery (n=10), the common carotid artery (n=10), the abdominal aorta (n=4) and the renal artery (n=4). 20 patients with TA were operated on. 17 of them underwent arterioarterial bypass, and 5 patients received angioplasty. There were 8 cases of reoperation due to the effect on other arteries, or due the stenosis or occlusion of the previous bypass graft. Angioplasty and stenting can be used in the treatment of shorter stenoses such as those encountered in the renal arteries. CONCLUSION: Symptomatic patients who have Takayasu's arteritis can be operated on. Our surgical experiences have showed low mortality and the surgical procedures relieved the symptoms. Surgical therapy for Takayasu's arteritis was safe and it showed good results.


Sujets)
Femelle , Humains , Mâle , Anévrysme , Angioplastie , Aorte , Aorte abdominale , Artères , Asiatiques , Artère axillaire , Artères carotides , Artère carotide commune , Sténose pathologique , Artère rénale , Réintervention , Études rétrospectives , Endoprothèses , Artère subclavière , Maladie de Takayashu , Transplants
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