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1.
Journal of the Korean Society for Surgery of the Hand ; : 161-166, 2009.
Artigo em Coreano | WPRIM | ID: wpr-21046

RESUMO

PURPOSE: The vessels of the finger tip are very small and fragile, have many branches, so the anastomosis of this vessel is very difficult. Guillotine type amputation of digits are rare, on the other hand, crush/avulsion injuries which require complex surgical solutions are more frequent. We often found that the arteries of distal amputee on crush/avulsion injuries are lost. In these cases, replantation is much more difficult even impossible. But when replantation is successes, the replantated finger tip provides adequate soft tissue, restoration of length, sensory and nail. MATERIALS AND METHODS: We report here our experience of finger tip replantation using afferent a-v anastomosis technique accumulated from March 2006 to March 2009. RESULT: The success rate was 96.4%. Complications occurred in eight patients. (5 digit atrophy, 1 osteomyelitis, 1 severe digit pain and 1 cold intolerance) CONCLUSIONS: We believe that the afferent a-v anastomosis replantation provides us wider range of indication of finger tip replantation on crush/avulsion injuries.


Assuntos
Humanos , Amputação Cirúrgica , Amputados , Artérias , Anastomose Arteriovenosa , Atrofia , Temperatura Baixa , Dedos , Glicosaminoglicanos , Mãos , Osteomielite , Reimplante
2.
Korean Journal of Gynecologic Oncology ; : 160-164, 2007.
Artigo em Coreano | WPRIM | ID: wpr-87029

RESUMO

Non-Hodgkin's lymphoma presented as a malignancy of the uterine cervix is exceedingly rare disease and accounts for approximately only 0.12-0.6% of extranodal lymphomas. There is no consensus on the management and prognosis of the disease because of its extreme rarity. Previously, treatment of this disease has been radiation therapy, surgery or chemotherapy either alone or in combination. We present the case of a 45-year-old woman diagnosed with diffuse, large B-cell non-Hodgkin's lymphoma of the uterine cervix. We administered neoadjuvant chemotherapy according to CHOP protocol (cyclophosphamide, adriamycin, vincristine, and prednisone) followed by hysterectomy and bilateral salpingo-oophorectomy. The patient is alive 20 months after the initial diagnosis. We report the case with a brief review of literature.


Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Linfócitos B , Colo do Útero , Consenso , Diagnóstico , Doxorrubicina , Tratamento Farmacológico , Histerectomia , Linfoma , Linfoma não Hodgkin , Prognóstico , Doenças Raras , Vincristina
3.
Korean Journal of Obstetrics and Gynecology ; : 1138-1142, 2006.
Artigo em Coreano | WPRIM | ID: wpr-53985

RESUMO

Endodermal sinus tumor (EST) is a rare malignant germ cell tumor arising usually in the gonads such as the testis or ovary. However, 10-15% of EST cases may arise in the extragonadal sites, such as sacrocoxygeal area, mediastinum, vagina, brain and retroperitoneum in a frequent occurring order. To our knowledge there are only 2 case reports of extragonadal EST, one originating from the omentum in 1998, and another which was localized in the pelvis in 2003. We report one case of extragonadal sinus tumor which arose in appendix and mesentery in the 19-year-old female with a review of the literature.


Assuntos
Feminino , Humanos , Adulto Jovem , Apêndice , Encéfalo , Endoderma , Tumor do Seio Endodérmico , Gônadas , Mediastino , Mesentério , Neoplasias Embrionárias de Células Germinativas , Omento , Ovário , Pelve , Testículo , Vagina
4.
Korean Journal of Obstetrics and Gynecology ; : 2194-2198, 2006.
Artigo em Coreano | WPRIM | ID: wpr-16768

RESUMO

Meckel Gruber syndrome consisting of an occipital encephalocele, polycystic kidney disease and polydactyly is a rare autosomal recessive disorder with a recurrence risk of 25%. Targeted ultrasonography in late embryonic or early fetal stages of pregnancy has great importance in diagnosis and management of affected pregnancy in high risk groups due to incomplete genetic mapping of meckel syndrome gene (MKS). We present a case of prenatal diagnosis at 14 weeks' gestational age of Meckel Gruber syndrome in a woman, who experienced same disorder in her previous pregnancy.


Assuntos
Feminino , Humanos , Gravidez , Diagnóstico , Encefalocele , Idade Gestacional , Doenças Renais Policísticas , Polidactilia , Diagnóstico Pré-Natal , Recidiva , Ultrassonografia
5.
Korean Journal of Obstetrics and Gynecology ; : 2198-2204, 2005.
Artigo em Coreano | WPRIM | ID: wpr-209218

RESUMO

OBJECTIVE: Endometriosis is assumed to be one of the causes of infertility, although the mechanism remains unclear. The purpose of this study was to determine the prognostic factors for the fertility in women with severe endometriosis. METHODS: Clinical data of 78 consecutive infertile patients who had taken surgery for stage III and IV endometriosis were retrospectively analyzed in two groups: A- pregnant after surgery (n=43, 55.1%): B- non-pregnant after surgery (n=35, 44.9%). All patients were treated with GnRHa after surgery. Each group were compared age, BMI, duration of infertility, stage of endometriosis, size and number of endometrioma, peritoneal implant outside the pelvic cavity, peritubal adhesion, ovarian adhesion and cul-de-sac obliteration. RESULTS: Among these factors, duration of infertility (p=0.03), peritoneal implant (p=0.01), tubal adhesion (p=0.04) and ovarian adhesion (p=0.02) were significantly different. However, patients' age, BMI, size and number of endometrioma, cul-de-sac obliteration and stage of endometriosis did not showed significantly different. CONCLUSION: We concluded that the duration of infertility and tubal and ovarian adhesion are important factors for predicting pregnancy after surgery in severe endometriosis.


Assuntos
Feminino , Humanos , Gravidez , Endometriose , Fertilidade , Infertilidade , Estudos Retrospectivos
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