• Title/Summary/Keyword: Malignant transformation.

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Laparoscopic Ovary Preserving Cystectomy forBenign Cystic Teratoma of the Ovary (소아 난소 양성 낭기형종 환자의 복강경적 난소 보존 낭종절제술)

  • Park, Il-Kyung;Mok, Woo-Kyun
    • Advances in pediatric surgery
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    • v.12 no.1
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    • pp.41-46
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    • 2006
  • Mature cystic teratoma, commonly called dermoid cyst, is the most common benign germ cell tumor of the ovary in children. Malignant transformation is rare, approximately 2 %. As laparoscopic procedures are applied widely in pediatric surgery, a female chlid with a mature cystic teratoma may be an ideal candidate for laparoscopic surgery. Two children received laparoscopic operations successfuly for lower abdominal crises, twisted adnexa. There was no operative complication. Laparoscopic approach for ovarian lesions in infancy and childhood appears to be an effective and safe method for diagnosis as well as definitive therapy.

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Tumor targeted gene therapy (종양 표적 유전자 치료)

  • Kang, Joo-Hyun
    • Nuclear Medicine and Molecular Imaging
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    • v.40 no.5
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    • pp.237-242
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    • 2006
  • Knowledge of molecular mechanisms governing malignant transformation brings new opportunities for therapeutic intervention against cancer using novel approaches. One of them is gene therapy based on the transfer of genetic material to an organism with the aim of correcting a disease. The application of gene therapy to the cancer treatment has led to the development of new experimental approaches such as suicidal gene therapy, inhibition of oncogenes and restoration of tumor-suppressor genes. Suicidal gene therapy is based on the expression in tumor cells of a gene encoding an enzyme that converts a prodrug into a toxic product. Representative suicidal genes are Herpes simplex virus type 1 thymidine kinase (HSV1-tk) and cytosine deaminase (CD). Especially, physicians and scientists of nuclear medicine field take an interest In suicidal gene therapy because they can monitor the location and magnitude, and duration of expression of HSV1-tk and CD by PET scanner.

Prolonged Air Leakage Caused by Mesenchymal Cystic Hamartoma of the Lung

  • Lee, Young Uk;Lee, Jang Hoon;Baek, Jong Hyun
    • Journal of Chest Surgery
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    • v.49 no.4
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    • pp.302-305
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    • 2016
  • A 16-year-old girl was transferred to the department of thoracic and cardiovascular surgery because of a spontaneous pneumothorax with prolonged air leakage. Chest computed tomography demonstrated a cystic lesion measuring $2{\times}3cm$ and involving the left upper lobe. Left upper lobectomy was performed via video-assisted thoracoscopic surgery. A pathologic examination of the specimen revealed a mesenchymal cystic hamartoma. Despite the rarity of pulmonary mesenchymal cystic hamartoma, it should be considered a potential cause of pneumothorax for patients with a large pulmonary cyst. Further, surgical resection must be considered because serious complications such as hemothorax, hemoptysis, and malignant transformation have been reported.

Current Insights on Cholangiocarcinoma Research: a Brief Review

  • Mathema, Vivek Bhakta;Na-Bangchang, Kesara
    • Asian Pacific Journal of Cancer Prevention
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    • v.16 no.4
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    • pp.1307-1313
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    • 2015
  • Colangiocarcinoma (CCA) is a progressively fatal disease which generally occurs due to malignant transformation of hepatic biliary cholangiocytes. The incidence of CCA has been increasing worldwide and there is an urgent requirement for effective diagnosis and treatment strategies against this devastating disease. Different factors including liver-fluke infestation, viral hepatitis, exogenous nitrosamine-mediated DNA damage, and chronic inflammation have been linked to CCA genesis. However, the risk factors and underlying complex mechanisms leading to development of CCA are not sufficiently understood to devise an effective targeted treatment therapy. In this review, we summarize currently known epidemiological and pathological aspects of the disease and briefly describe various potential biomarkers and experimental anticancer phytochemicals related to CCA research. In addition, we also sum up recent findings that link chronic inflammation of hepatic biliary cholangiocytes with CCA. The collective information concisely presented in this article would provide useful insights into the current understanding of this cancer.

Hallux Rigidus with Osteochondroma of the Hallucal Proximal Phalanx (A Case Report) (족무지 근위지절 골연골종과 동반한 무지 강직증 (증례보고))

  • Chae, Soo Uk;Kim, Yeung Jin;Jo, Hyang Jeong;Choi, Deok Hwa;Cha, Myoung Soo
    • Journal of Korean Foot and Ankle Society
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    • v.17 no.1
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    • pp.60-63
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    • 2013
  • Small osteophytes are frequently encountered in the foot and ankle, and not to be confused with true osteochondromas, which are relatively uncommon in this region. Osteochondromas are the most common benign osseous neoplasm, occurs in the metaphysis of the long bone. It is rarely found in bones of the foot. Treatment of the osteochondroma is usually conservative, unless symptoms usually pain, are progressive rapid growth, and malignant transformation is suspected. We experienced a rare case of hallux rigidus with osteochondroma of the hallucal proximal phalanx which cause pain and corn of the plantar.

Elastofibroma Dorsi - A case report - (흉벽에 발생한 탄성섬유종 - 1예 보고 -)

  • 김병호;허동명;손경락;신현웅
    • Journal of Chest Surgery
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    • v.36 no.4
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    • pp.293-296
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    • 2003
  • Elastofibroma, dorsi, a rare, noncapsulated benign entity is characterized by the proliferation of fibrous tissue with elastin and occurs most often in the infrascapular area of elderly women. It is a relatively slowly growing lesion and no reports of malignant transformation exist. Which is overlooked easily because it rarely causes symptoms such as tenderness, pain, or restriction of movement. The diagnosis of elastofibroma is established by typical histopathologic findings. Radiographic evaluation may lead to a presumptive diagnosis. We experienced a case of elastofibroma dorsi in a 48-year-old woman and report this case with a review of the literature.

Non-Redundancy within the RAS Oncogene Family: Insights into Mutational Disparities in Cancer

  • Lau, Ken S.;Haigis, Kevin M.
    • Molecules and Cells
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    • v.28 no.4
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    • pp.315-320
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    • 2009
  • The RAS family of oncoproteins has been studied extensively for almost three decades. While we know that activation of RAS represents a key feature of malignant transformation for many cancers, we are only now beginning to understand the complex underpinnings of RAS biology. Here, we will discuss emerging cancer genome sequencing data in the context of what is currently known about RAS function. Taken together, retrospective studies of primary human tissues and prospective studies of experimental models support the notion that the variable mutation frequencies exhibited by the RAS oncogenes reflect unique functions of the RAS oncoproteins.

EFFECTS OF THE SOY ISOFLAVONE GENISTEIN ON COX-2 EXPRESSION AND ACTIVATION OF ERKl/2 INDUCED BY PHORBOL ESTER AND TNF-$\alpha$ IN HUMAN BREAST EPITHELIAL CELL LINE (MCF10A)

  • Chung, Myung-Hoon;Kim, Jung-Hwan;Lee, Seung-Sei;Keum, Joo-Seob;Surh, Young-Joon
    • Proceedings of the Korean Society of Toxicology Conference
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    • 2001.10a
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    • pp.135-136
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    • 2001
  • Genistein has been shown to exert propective effects against chemically induced carcinogenesis in animals as well as malignant transformation in cultured cells, but molecular mechanisms of its chemopreventive or chemoprotective activities remain largely unresolved. In the present sturdy, we have investigated the effects of genistein on induction of cyclooxygenase-2 (COX-2) that plays an important role in the pathophysiology of carcinogenesis as well as in cellular response to inflammatory stimuli.(omitted)

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Bronchogenic Cyst Presenting as an Posterior Pharyngeal Mass (성인에서 후인두에 발생한 기관지원성 낭종 1예)

  • Yun, Seong Hyun;Choi, Ha Na;Seo, Jae Hyun;Park, Young-Hak
    • Korean Journal of Bronchoesophagology
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    • v.18 no.2
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    • pp.64-66
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    • 2012
  • Bronchogenic cysts are uncommon congenital anomalies and commonly located in the mediastinum or lung parenchyma. Bronchogenic cyst in cervical area is rare and in posterior pharyngeal area is exteremely rare. Clinically, it is usually asymptomatic and incidentally diagnosed. It is pathologically confirmed only when there are bronchial tissues such as pseudostratified ciliated columnar epithelium, smooth muscle cells, mucous gland and/or cartilage. Since it has potential for malignant transformation and complication, complete excision is essential. We report a case of bronchogenic cyst located in the retropharyngeal space with a review of literature.

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Killian-Jamieson diverticulum lined with two epithelia in a Korean cadaver

  • Cha, Min-Kyoung;Kang, Seung Weon;Maeng, Young Hee;Kim, Jinu;Yoon, Sang-Pil
    • Anatomy and Cell Biology
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    • v.51 no.4
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    • pp.299-301
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    • 2018
  • Killian-Jamieson diverticulum is a permanent protrusion of anterolateral proximal esophagus through anatomically weak muscular gap, known as Killian-Jamieson area, into adjacent area. During a routine educational dissection, we found a well-defined lateral diverticulum just inferior to the transverse fibers of the cricopharyngeus muscle in a Korean male cadaver. It had a dimension of $1.8{\times}1.4{\times}1.0cm$ with two types of epithelial cells, stratified squamous and simple cuboidal to low-columnar epithelium, and attenuated and haphazardly arranged muscle fibers. No epithelial dysplasia or malignant transformation was identified except ulcerative changes. Although Killian-Jamieson diverticulum is a very rare disease, clinicopathological aspects should be considered.