• 제목/요약/키워드: Cystic hygroma

검색결과 32건 처리시간 0.017초

소아에서 발생한 비치성 양성종양에 관한 임상적 연구 (A CLINICAL STUDY OF THE NON-ODONTOGENIC BENIGN TUMORS OCCURRED IN THE CHILDREN)

  • 김영신;허선;김문현;김재곤;백병주
    • 대한소아치과학회지
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    • 제25권2호
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    • pp.458-466
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    • 1998
  • Non-odontogenic tumors can be classified as malignant or benign. Most oral tumors in children are benign. In the Belfast series only 7.5 percent of soft tissue tumors were malignant and Bhaskar(l963) found only 9 percent of 293 oral tumors of all kinds to be malignant. Benign tumors may be classified as epithelial and mesenchymal. The most common tumor of surface epithelium is the squamous papilloma. These are easily recognized clinically as cauliflower-like lesions. Fibrous lesions are very common in children's mouths. Many of these are not true neoplasms but are related to fibrous hyperplasia. Another common oral tumor in children is angiomatous tumors. Hemangioma occurred more frequently than lymphangioma. Cystic hygroma, a cystic subtype of lymphangioma, is a developmental tumor of lymphatic origin. It is a considered to be a relatively rare lesion. About 50 percent of cystic hygroma are present at birth, and most of the remaining 50 percent appear in the early years of life during the period of active lymphatic growth. The preferred treatment for these lesions, except for hemangioma, is complete surgical excision. With proper surgical techniques, recurrence is not expected.

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성인에서 발생한 흉벽 낭포성림프관종 (Cystic Lymphangioma in the Chest Wall of an Adult)

  • 김재호;윤용한;김정택;백완기;이경희;김루시아;김광호
    • Journal of Chest Surgery
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    • 제40권7호
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    • pp.523-525
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    • 2007
  • 낭성활액낭종으로도 불리는 낭포성림프관종은 보통 경부와 액와부에 잘 발생하고 출생 시부터 발견되며, 90% 이상의 환자에서 늦어도 2세 이전에 발견된다. 성인의 흉벽에서 발견되는 예는 아주 드문 경우로 알려져 있다. 저자들은 64세의 남자 환자에서 좌 후흉벽에 발생한 낭성림프관종을 치험하였기에 보고하는 바이다.

종격동 임파관종;1례 보고 (Mediastinal lymphangioma - 1 Case -)

  • 이해영
    • Journal of Chest Surgery
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    • 제25권10호
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    • pp.1112-1115
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    • 1992
  • Lymphangioma, or cystic hygroma, a malformation resulting from the sequestration of lymph vessels, is owing to a failure of the primitive jugular lymphatic sacs to join with the venous system. They are rare benign lesions found more frequently in children than in adults. We experienced a case of huge mediastinal lymphangioma in 37-year-old female patient. It was associated with a cervical prolongation, and caused deviation and compression of the trachea and the heart. The cervicomediastinal lymphangioma was completely resected by means of median sternotomy, and the post-operative course was unevenful.

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종격동내 위치한 갑상선 내 갑상설관 낭종: 증례 보고 및 문헌 고찰 (Intrathyroid Thyroglossal Duct Cyst Extending into the Mediastinum: A Case Report and Review of Literature)

  • 이찬미;홍용태
    • 대한두경부종양학회지
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    • 제38권1호
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    • pp.65-68
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    • 2022
  • Thyroglossal duct cyst (TGDC) is the most common congenital cyst in the neck and usually presents in children. It is most commonly located at the infrahyoid level. However, intrathyroid TGDC in the adult is extremely rare and its pathogenesis remains unclear. Curiously, an intrathyroid TGDC was found on the lateral aspect of the inferior pole of the thyroid gland. Given the unique position of this lesion, and its capacity to stimulate other nodules in the thyroid, it should be differentiated from other lateral neck masses, such as: thymic cysts, branchial cleft cysts, cystic hygroma, lipomas, lymphadenopathies, cervical teratomas, and lymphomas. In this case, a separate cystic mass was found in the right inferior pole of the thyroid gland and extended to the mediastinum. We confirmed it as TGDC by pathology and histological examination.

측경부 낭종으로 발현된 유두상 갑상선암 (Lateral Neck Cyst as the Initial Presentation of Papillary Thyroid Carcinoma)

  • 박정수;이원흥;김춘규
    • 대한두경부종양학회지
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    • 제4권1호
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    • pp.53-58
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    • 1988
  • We have experienced 3 cases of papillary carcinoma of the thyroid gland seen as lateral neck cyst, Usually cystic lesions of the neck have been considered as benign lesions from clinical viewpoint. The usual differential diagnosis includes branchial cleft cyst, cystic hygroma, dermoid cyst, cold abscess(tuberculous lymphadenitis) and cavitating squamous cell carcinoma. A lateral neck cyst as the sole presenting complaint of the papillary thyroid carcinoma is very rare. Preoperative diagnosis of lateral neck cyst is often diagnostic dilemma. Fine-needle aspiration cytology can be helpful in detecting the cancer cells and in demonstrating the nature of the fluid component of the lateral neck cyst. Presence of brown murky fluid from the aspirated fluid is highly suggestive of thyroid carcinoma. The thyroid scans and B-mode ultrasonography mayor may not be helpful to detect the primary focus of the thyroid gland. We suggest that a patient with a lateral neck cyst in adult age group should be considered to be a possibility of underlying thyroid carcinoma presanting as lateral neck cyst.

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소아 림프관종의 임상적 특징과 치료 (Clinical Manifestation and Treatment of Lymphangioma in Children - a Review of 117 Cases -)

  • 강계수;정풍만
    • Advances in pediatric surgery
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    • 제8권2호
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    • pp.95-100
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    • 2002
  • Lymphangiomas or cystic hygromas are quite commonly seen in children. During a 22-year period, from January 1980 to December 2001, 117 patients with lymphangioma were treated and followed in the Department of Pediatric Surgery at Hanyang University Hospital. The male-to-female ratio was 1.9:1(77:40) with a male preponderance. As for the age incidence at time of diagnosis, 10(8.5 %) patients were noted under 1 month of age, 37(31.6%) were between 1 month and 1 year of age, 12(10.3%) between 1 and 2 years of age, so 59(50.4%) were under 2 years of age. Sixty one (52.1%) lymphangioma-cases were located in the neck, including one case at the nape. Axilla was the second in frequency and the rest were scattered at various sites. The intrascrotal lymphangioma is very rare but we have experienced one case of primary intrascrotal lymphangioma. Eighteen (15.4%) cases were located in the intraabdominal area, 10 in the mesentery, 2 in the greater omentum and 6 in the retroperitoneum. The chief complaints of intraabdominal lymphangioma were abdominal pain, intestinal obstruction, inguinal hernia, palpable mass, and/or abdominal distension. Among 77 histologically proven cases, 14 cases were cavernous lymphangiomas and the rest were cystic lymphangiomas. Bleeding in the lymphangioma was noted in 20(17.1%) cases of all. As for the treatment, a complete excision was performed in 77(65.8%) patients and $AgNO_3$ sclerotherapy after incomplete excision was performed in 23(19.7%). Picibanil (OK-432) sclerotherapy was performed in 17(14.5%) patients. Recurrence rate was 7.7 % and mortality occurred in one case who had a large neck lymphangioma extending into the mediastinum.

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경부 및 상부종격동에 발생한 낭상임파관종 1례 (Cervicomediastinal cystic hygroma: report of a case)

  • 서충헌
    • Journal of Chest Surgery
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    • 제13권4호
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    • pp.503-506
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    • 1980
  • A 37 year old male patient was suffered from severe labored breathing caused by post tracheostomy stenosis, which was localized at the mediastinal trachea [cuffed tracheal stenosis] and ranged 1.5 cm in length and approximately 3 ram. in diameter on tracheogram. After dilation of tracheal stenosis with dilator, endotracheal intubation was tried for induction of anesthesia and control of respiration during operation. A tube was placed just beyond the tracheal stenosis without respiratory difficulty. Under the endotracheal anesthesia, circumferential resection of the mediastinal trachea containing the stenosis, approximately 2 cm in length [4 tracheal rings}, was carried out and primary direct end to end anastomosis was performed with interrupted submucosal sutures [3-0 Dexon] and mobilization of trachea Postoperative tracheostomy was not performed. The patient was completely relieved from dyspnea immediately after operation. Post-operative convalescence was entirely uneventful and at present, about 3 months after operation, he is now conducting a usual life. From the literature and our experience, the etiology and treatment of post-tracheostomy stenosis were discussed.

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흉벽의 임파관종 (Lymphangioma of the Chest Wall)

  • 김영진;이철주;소동문;김정태;강준규;홍준화
    • Journal of Chest Surgery
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    • 제32권9호
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    • pp.855-857
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    • 1999
  • 흉벽의 임파관종은 전 세계적으로 매우 드물게 보고 되어있다. 본원에서는 16세의 여자환자로 우측 상부 후측방 흉벽에 반복적으로 나타나는 거대 종괴를 주소로 내원한 임파관종 환자를 치험하였다. 진단은 이학 적 검사와 흉부 핵자기공명 촬영, 동위원소 임파관 촬영술을 실시하였으며 조직검사로 확진하였다. 치료는 외과적 완전 절제를 하였으며 술후 반복적 림프액의 유출로 수술부위에 vibramycin을 주사하였다.

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양성(良性) 종격동(縱隔洞) 종진(腫疹)의 외과적(外科的) 치료(治療) (Surgical Treatment of Benign Mediastinal Tumor)

  • 김병노
    • Journal of Chest Surgery
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    • 제9권1호
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    • pp.83-89
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    • 1976
  • This is a report on the cases of benign mediastinal tumors in the Department of Thoracic and Cardiovascular Surgery, Chonnam University Hospital during the period from 1961 to 1975. Age distribution was from 18 to 62 years old with the highest incidence in the 3rd decade, and sex ratio of male to female was 7 : 8. The tumor were classified as follows; 6 cases of teratoma 5 cases of neurogenic tumor one case of pericardial cyst one case of cystic hygroma one case of dermoid cyst one case of bronchogenic cyst. The symptomatic patients were 10 cases (66.7%) and asymptomatic patients were 5 cases (33.3%), who were found incidentally by routine chest n-ray. The symptoms occurred by compression to the adjacent nerve system in 7 cases, by perforation into the lung with infection in one case of teratoma and by infection of bronchogenic cyst in one case and of teratoma in one case. Complications were Pancoast's syndrome including Horner's syndrome 2 cases, middle lobe syndrome 2 cases, intercostal neuralgia 1 case and bronchitis 1 case. All tumors were surgically resectable with good recovery. In all 10 cases of symptomatic patients, their symptoms disappeared dramatically after operation.

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Multiloculated Hydrocephalus : Open Craniotomy or Endoscopy?

  • Lee, Yun Ho;Kwon, Young Sub;Yang, Kook Hee
    • Journal of Korean Neurosurgical Society
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    • 제60권3호
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    • pp.301-305
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    • 2017
  • Multiloculated hydrocephalus (MLH) is a condition in which patients have multiple, separate abnormal cerebrospinal fluid collections with no communication between them. Despite technical advancements in pediatric neurosurgery, neurological outcomes are poor in these patients and the approach to this pathology remains problematic especially given individual anatomic complexity and cerebrospinal fluid (CSF) hydrodynamics. A uniform surgical strategy has not yet been developed. Current treatment options for MLH are microsurgical fenestration of separate compartments by open craniotomy or endoscopy, shunt surgery in which multiple catheters are placed in the compartments, and combinations of these modalities. Craniotomy for fenestration allows better visualization of the compartments and membranes, and it can offer easy fenestration or excision of membranes and wide communication of cystic compartments. Hemostasis is more easily achieved. However, because of profound loss of CSF during surgery, open craniotomy is associated with an increased chance of subdural hygroma and/or hematoma collection and shunt malfunction. Endoscopy has advantages such as minimal invasiveness, avoidance of brain retraction, less blood loss, faster operation time, and shorter hospital stay. Disadvantages are also similar to those of open craniotomy. Intraoperative bleeding can usually be easily managed by irrigation or coagulation. However, handling of significant intraoperative bleeding is not as easy. Currently, endoscopic fenestration tends to be performed more often as initial treatment and open craniotomy may be useful in patients requiring repeated endoscopic procedures.