• 제목/요약/키워드: girl

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변색된 치아의 심미성 회복에 관한 임상증례 (ESTHETIC IMPROVEMENT OF DISCOLORED TEETH : A CASE REPORT)

  • 정호석;김대업
    • 대한소아치과학회지
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    • 제21권2호
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    • pp.593-598
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    • 1994
  • There were two cases of esthetic improvement of discolored teeth. First case was 12-year-old girl whose upper right central incisor was discolored after traumatic injury. She was treated by walking bleaching technique. Endodontic retreatment was done, and then the mixture of Superoxol and sodium perborate was applied and changed every week. After 3 weeks, esthetic result was obtained and fracture site was rcovered with light-curing composite resin. Second cases was 11-year-old girl whose teeth were discolored by fluorosis. She was treated by vital bleaching technique. A resin splint was made and then 30% and 15% carbamide peroxide was applied using this splint. After 4 weeks, a noticeable improvement in the color and the brightness of the teeth was achieved.

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Deep Brain Stimulation of the Globus Pallidus in a 7-Year-Old Girl with DYT1 Generalized Dystonia

  • Jin, Seon Tak;Lee, Myung Ki;Ghang, Ju Young;Jeon, Seong Man
    • Journal of Korean Neurosurgical Society
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    • 제52권3호
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    • pp.261-263
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    • 2012
  • The experience of pediatric deep brain stimulation (DBS) of the globus pallidus internus (GPi) in the treatment of early-onset DYT1 generalized dystonia is still limited. Here, we report the surgical experience of bilateral GPi-DBS under general anesthesia by using microelectrode recording in a 7-year-old girl with early-onset DYT1 generalized dystonia. Excellent improvement of her dystonia without neurological complications was achieved. This case report demonstrates that GPi-DBS is an effective and safe method for the treatment of medically refractory early-onset DYT1 generalized dystonia in children.

A case of pyogenic liver abscess in a 10-year-old girl

  • Byun, Jung-Lim;Bae, Sun-Hwan;Park, Sang-Woo
    • Clinical and Experimental Pediatrics
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    • 제53권5호
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    • pp.666-668
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    • 2010
  • Pyogenic liver abscesses are rare in children. In pediatric patients, altered host defences seem to play an important role. However, pyogenic liver abscess also occurs in healthy children. We experienced a case of pyogenic liver abscess in a healthy immunocompetent 10-year-old-girl. The patient presented two distinct abscesses: one subphrenic and the other intrahepatic. The intrahepatic abscess resolved with percutaneous drainage and 3 weeks of parenteral antibiotic therapy but the subphrenic abscess which could not be drained needed prolonged parenteral antibiotic therapy in addition to oral antibiotic therapy. We performed follow-up serial CT scan of the abscess cavity to decide on the duration of antibiotic therapy. Here we present this case with a brief review of the literature.

Severe Hypophosphatemia in a Girl with Systemic Lupus Erythematosus

  • Lim, Taek Jin;Kim, Su Young;Kim, Seong Heon
    • Childhood Kidney Diseases
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    • 제21권2호
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    • pp.156-159
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    • 2017
  • Systemic lupus erythematosus (SLE) is characterized by various symptoms and multi-organ involvement. Hypophosphatemia has been described in several diseases accompanied with systemic inflammation. However, hypophosphatemia has rarely been described in SLE patients, especially in those without nephritis. We report the case of a 13-year-old girl with SLE who developed hypophosphatemia without renal involvement. Her hypophosphatemia was caused by renal loss of phosphorus and persisted for 7 months. It improved as her complement levels increased. Therefore, hypophosphatemia may be related to disease activity in SLE patients.

Spontaneous Chronic Subdural Hematoma in an Adolescent Girl

  • Wang, Hui Sun;Kim, Seok Won;Kim, Sung Hoon
    • Journal of Korean Neurosurgical Society
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    • 제53권3호
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    • pp.201-203
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    • 2013
  • In most cases, subdural hematoma (SDH) is regarded as a complication of head injury and nontraumatic causes are rare. Moreover, spontaneous chronic SDH in child or adolescent is very unusual. Here, we present the case of a healthy 14-year-old girl who was diagnosed as a spontaneous chronic SDH. The patient presented with severe headache following blurring of vision two weeks ago without any history of trivial head injury. Computed tomography and magnetic resonance imaging depicted a chronic SDH. The cause of the hematoma was not established. After performing burr hole drainage of the hematoma, the patient made an uneventful recovery. We explore the potential risk factors and pathophysiology implicated in this condition. Possible pathogenic mechanisms of this unique case are discussed and a review of the pertinent literature is included.

인삼을 찌는 것과 삶는 것의 차이 (Difference between Steaming and Decocting Ginseng)

  • 박서영;정일;강탁림;박만기
    • Journal of Ginseng Research
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    • 제25권1호
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    • pp.37-40
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    • 2001
  • 수증기로 찐 다음 뜨거운 물로 추출한 인삼 추출물과 뜨거운 물로만 추출한 인삼 추출물을 대상으로 갈변화 정도와 라디칼 소거활성을 검토하였다. 그결과 수증기로 찌는 것이 물속에서 가열하는 것보다 갈변화 반응이 더 많이 진행되며, 그 추출물의 항산화작용도 더 크다는 것을 알 수 있었다. 이러한 차이는 수삼보다 백삼을 원료로 사용한 경우가 더 큰 것으로 나타났다.

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Solitary Atypical Adenomatous Hyperplasia in a 12-Year-Old Girl

  • Jin, Moran;Lee, Yang-Haeng;Kim, Bomi;Yoon, Young Chul;Wi, Jin Hong
    • Journal of Chest Surgery
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    • 제49권2호
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    • pp.141-144
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    • 2016
  • Atypical adenomatous hyperplasia is a premalignant lesion reflecting a focal proliferation of atypical cells. These lesions are usually observed as incidental findings in lungs that have been resected due to other conditions, such as lung cancer. We report the youngest case of atypical adenomatous hyperplasia on record in a 12-year-old girl. In this patient, the lesion was found in association with pneumothorax.

Rapid-Growing Juvenile Xanthogranuloma on the Scalp in 18-Month-Old Girl

  • Park, Young-Woo;Koh, Eun-Jeong;Choi, Ha-Young
    • Journal of Korean Neurosurgical Society
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    • 제50권3호
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    • pp.271-273
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    • 2011
  • Juvenile xanthogranuloma (JXG) is an uncommon histiocytic cutaneous lesion. An 18-month-old girl visited our clinic due to rapid growing orange-yellowish lesion on scalp. Enlarging time from 1 mm to 12 mm was just 8 weeks. We excised the tumor and adjacent normal tissue. Histopathological study showed numerous eosinophils and Touton giant cells within the lesion. Immunohistochemical study revealed positive immunoreactivity for CD68 in most areas. No recurrence was seen during 12 months after resection. We report a case with rapidly growing JXG on scalp with peculiar histopathologic findings.

소아에서 피하매몰 중심정맥포트가 전복된 사례에 대한 경험 - 2예 보고 - (Inversion of Implantable Central Venous Port in Children - 2 Cases Report -)

  • 최준영;김현영;정성은;박귀원;김우기
    • Advances in pediatric surgery
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    • 제12권1호
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    • pp.17-23
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    • 2006
  • A 3-year-old girl with a primitive neuroectodermal tumor (PNET) and a 6-yearold girl with acute lymphoid leukemia were referred to us because of problems with their implantable central venous ports (Port-A-Cath$^{(R)}$). On physical examination, the ports were upside-down, so a needle could notbe inserted through the membrane of the port. Right lateral side view of the chest radiogram confirmed port inversion in both cases. At operation, the ports were inverted and the transfixing sutures were totally absorbed. The ports were rotated 180 degrees and anchoring sutures placed.

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4세 영아의 난소에서 발생한 Sertoli-Leydig 세포 종양 -1예 보고- (Sertoli-Leydig Cell Tumor of the Ovary in a 4 year-old Girl - A Case Report -)

  • 김혜진;최병호;박진영
    • Advances in pediatric surgery
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    • 제15권1호
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    • pp.73-79
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    • 2009
  • Sertoli-Leydig cell tumor is a rare sex-cord stromal tumor of the ovary. They make up less than 0.5 % of all ovarian tumors. We experienced a case of an ovarian Sertoli-Leydig cell tumor in a 4 year-old girl who presented with nausea, vomiting, and lower abdominal pain of 2 days' duration. On physical examination, there was mild tenderness in the right lower quadrant of the abdomen. Abdominal ultrasonography and computed tomography (CT) scan revealed a pelvic mass measuring $5{\times}3cm$ that appeared to arise from the right ovary. At exploratory laparotomy, a $6{\times}5{\times}3cm$ solid right ovarian mass without torsion was found. A right salpingo-oophorectomy was performed. The postoperative course was uneventful. The child was discharged 5 days after surgery.

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