• 제목/요약/키워드: Giant-cell tumor

검색결과 169건 처리시간 0.023초

Stimulation of Osteogenic Differentiation in Stromal Cells of Giant Cell Tumour of Bone by Zoledronic Acid

  • Yang, Tao;Zheng, Xiao-Fei;Li, Mei;Lin, Xi;Yin, Qing-Shui
    • Asian Pacific Journal of Cancer Prevention
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    • 제14권9호
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    • pp.5379-5383
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    • 2013
  • Therapeutic effects of zoledronic acid (ZOL) on giant cell tumour of bone (GCT) have been proven. Apoptosis induction was considered to be one of the mechanisms of ZOL tumour inhibition. In this study, we presented the possibility of an osteogenic differentiation stimulation mechanism of ZOL and further investigated dosage and time effects. We treated stromal cells of GCT (GCTSC) with ZOL for 48 hours at different concentrations ($0{\mu}M$, $0.01{\mu}M$, $0.1{\mu}M$, $1{\mu}M$, 5${\mu}M$, $30{\mu}M$) and assessed apoptotic and osteogenic differentiation markers with immunohistochemical techniques and real-time quantitative RT-PCR. Our results suggested that ZOL enhanced mRNA expression of Cbfa-1, osterix and osteocalcin genes with a maximum effect at $1{\mu}M$ in GCTSC. Time course experiments indicated a time dependent osteogenic differentiation effect. In conclusion, ZOL may be considered as an adjuvant in the treatment of GCT not only by inducing apoptosis but also by stimulating osteogenic differentiation of remaining tumor stromal cells after surgery.

Central giant-cell granuloma in a patient with neurofibromatosis type 1: 7 years of follow-up

  • Michelle Briner Garrido;Rohan Jagtap;Christopher D. Matesi;Vivian Diaz;John Hardeman;Anita Gohel
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제50권1호
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    • pp.49-55
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    • 2024
  • Neurofibromatosis type 1 (NF1) is an autosomally dominant tumor suppressor syndrome and multisystem disease. Central giant-cell granulomas (CGCGs) can be seen in patients with NF1. A 21-year-old female was diagnosed with two CGCGs, one in the mandible and then one in the maxilla, in a 7-year period. Increased incidence of CGCGs in NF1 patients was thought to be caused by an underlying susceptibility to developing CGCG-like lesions in qualitatively abnormal bone, such as fibrous dysplasia. However, germline and somatic truncating second-hit mutations in the NF1 gene have been detected in NF1 patients with CGCGs, validating that they are NF1-associated lesions. Oral manifestations in patients with NF1 are very common. Knowledge of these manifestations and the genetic link between NF1 and CGCGs will enhance early detection and enable optimal patient care.

두피에 발생한 거대 피지샘 상피종 1례 (A Giant Sebaceous Epithelioma on the Scalp: A Case Report)

  • 김은연;김선구;김유진;이세일
    • 대한두개안면성형외과학회지
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    • 제13권1호
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    • pp.76-79
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    • 2012
  • Purpose: Sebaceous epithelioma (sebaceoma) is a benign tumor with sebaceous differentiation. It presents primarily as a yellowish papule or nodule on the face and scalp. It must be differentiated from basal cell carcinoma and other appendageal tumors. We report a giant sebaceous epithelioma on the scalp and describe the immunohistochemical character of the cells in sebaceous epithelioma to epithelial membrane antigen (EMA). Methods: A 55-year-old-man who presented with 5-cm-diameter 2-cm-height, round shape exophytic ulcerated tumor on his head presented for treatment. The patient had noticed the lesion 40 years prior as a small yellowish plaque and 18 months ago, the plaque started to grow progressively larger. We excised the lesion with 1 cm resection margin, considering the possibility of malignancy because this lesion grossly resembled basal cell carcinoma (BCC). The defect was repaired with the use of a splitthickness skin graft. Results: When we excised the lesion, the margin was clear. Histology showed nodules that consisted of an admixture of basaloid cells and mature adipocytes lacking an organized lobular architecture. Strong expression of EMA on mature adipose cells confirmed the differential diagnosis from BCC with sebaceous differentiation because of the absence of a nuclear palisade pattern and cleft-like spaces on the hematoxylin and eosin (H&E) section. Conclusion: We treated the giant sebaceous epithelioma on the scalp with surgical excision and a split-thickness skin graft. It is important to know that the diagnosis of sebaceous epithelioma should be made based on the histologic pattern of the H&E section. Immunohistochemistry with EMA can help to confirm the differential diagnosis between sebaceous epithelioma and BCC.

Characterization of Acharan Sulfate Binding Proteins in Murine Lewis Lung Carcinoma Cell

  • Joo, Eun-Ji;Hahn, Bum-Soo;Kim, Yeong-Shik
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.150.2-151
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    • 2003
  • We have focused on various biological activities of acharan sulfate (AS) isolated from the giant African snail Achatina fulica. In a previous study, AS showed antiangiogenic and immunomodulating activity. We also investigated antitumor activity of AS. In vitro AS had no cytotoxicity within 0 to 200 ug/ml in tumor cells such as Lewis lung carcinoma(LLC) , KM1214 (human colon cancer cell) and Caki-1 (human kidney cancer cell) by both MTT and SRB assay. In vivo AS was used to treat C57BL/6 mice bearing LLC by subscutaneous injection. (omitted)

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치은부에 발생한 거대세포육아종에 의한 골연화증 (TUMOR INDUCED OSTEOMALACIA : ASSOCIATED WITH GIANT CELL GRANULOMA ON THE GINGIVA)

  • 김여갑;류동목;이상철
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제13권2호
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    • pp.185-190
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    • 1991
  • 비내분비성 골종양이나 연조직종양에서 유래되는 구루병이나 골연화증은 매우 드문질환으로 1947 년 이래로 14 명의 환자만이 보고되고 있다. 이 질환의 본태는 아직 밝혀지지 않았으나 종양에서 생성하는 인산염뇨유발성 물질이 신세뇨관에 영향을 주고 저인산염혈증을 일으키며 골조직의 석회화에 장애를 일으키는 것으로 생각된다. 본 증례의 환자는 약 4 년 전부터 지속된 심한 전신동통과 근육위축, 현저한 신장의 감소를 주소로 내원한 41 세 남자로 상악우측 치은부의 종양에 의한 전신적 골연화증의 진단하에 종양의 외과적적출을 시행하였으며 술후 환자의 혈청과 뇨의 생화학적결과는 12 일 후에 정상으로 회복되었고 임상증상은 수술후 6 주에 회복되었으며 4 달후에 촬영한 치과 방사선상 놀랄만한 골재생과 새로 형성된 치조백선의 형성이 관찰되었다. 적출된 종물은 거대세포육아종의 조직소견을 보였으며 종물의 적출에 의하여 골연화증의 치유소견이 관찰 되었기에 종양에 의한 골연화증의 회유한 증례로 사료되어 이에 보고하는 바이다.

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동맥류성 골낭종으로 오인된 거골에 발생한 연골모세포종: 증례 보고 (Chondroblastoma of the Talus Mimicking an Aneurysmal Bone Cyst: A Case Report)

  • 박지수;서진수;최준영
    • 대한족부족관절학회지
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    • 제23권1호
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    • pp.31-34
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    • 2019
  • Chondroblastoma is a rare benign tumor that produces giant cells and cartilage matrix. The tumor occurs in people between 10 and 25 years with slightly higher incidence in males. The condition occurs in the proximal epiphysis of the tibia and humerus, distal epiphysis of the femur, but its occurrence in the talus is relatively rare, accounting for 4% of the total number of chondroblastoma cases. Chondroblastoma is often misdiagnosed as a primary aneurysmal bone cyst, giant cell tumor, chondromyxoid, and lesion of a secondary aneurysmal bone cyst by fibrous dysplasia. The most commonly used surgical method for chondroblastoma is broad curettage with bone grafting. In general, an aneurysmal bone cyst is associated with a second degree chondroblastoma, which is approximately 20%. Chondroblastoma of the talus and secondary aneurysmal bone cysts can be misdiagnosed as primary aneurysmal bone cysts. This paper reports a case of a young male patient with chondroblastoma of the talus, which was initially misdiagnosed as an aneurysmal bone cyst with involvement of the talo-navicular joint.

개에서 거대세포 치은종의 증례 (Peripheral Giant Cell Granuloma in a Dog)

  • 조은상;전성주;홍다해;류시윤;정주영;박배근;손화영
    • 한국임상수의학회지
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    • 제30권6호
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    • pp.478-481
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    • 2013
  • 18살의 암컷 푸들의 구강에서 종괴가 발견되었다. 육안적으로, 종괴는 단단하고, 적자색을 띠었으며, 크기는 $1.5{\times}1.5{\times}1cm$ 였다. 조직병리학적으로 종괴는 과증식된 잇몸 상피와 혈관이 잘 발달된 기질로 구성되어 있었으며, 다형 세포 및 퐁부한 호산성 세포질과 다수의 핵을 가진 많은 수의 거대 세포가 관찰되었다. 면역조직화학적으로, 종양 세포는 alkaline phosphatase와 cytokeratin 7에 양성 반응이었지만, CD68에 음성 반응이었다. 종괴는 전형적인 임상적, 조직병리학적인 특징에 의해 구강내 거대세포 치은종으로 진단되었다.

측경부에 발생한 방추세포 / 다형성 지방종1예 (A case of a Spindle cell/pleomorphic lipoma in the lateral neck)

  • 김영윤;윤성호;박종민;이동훈
    • 대한두경부종양학회지
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    • 제34권1호
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    • pp.41-43
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    • 2018
  • The Spindle cell lipoma is a slow-growing benign tumor seen generally in the shoulders, upper back, and back of the neck of male. The Pleomorphic (giant-cell) lipoma is a benign tumor of adipose tissue with atypical histological features. It is mainly seen in the same lesion as the Spindle cell lipoma. The Pleomorphic lipoma is cytogenetically similar to spindle cell lipoma with a consistent loss of chromosome 16q material. For this reason, these two entities are regarded as a similar spectrum in the adipose tumors. Herein, we present a 53-year old man with Spindle cell/pleomorphic lipoma in the lateral neck. Physical and radiologic examinations of the Spindle cell/pleomorphic lipoma in the lateral neck are not specific and preoperative diagnosis is usually difficult. Therefore, clinicians should consider the possibility that Spindle cell/pleomorphic lipoma may occur in the lateral neck mimicking the other more frequently observed lesions.

난소의 원발 투명세포암종의 세포소견 (Cytologic Findings of Clear Cell Carcinoma of Ovary)

  • 박지영;김혜선;최종순
    • 대한세포병리학회지
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    • 제17권1호
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    • pp.32-37
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    • 2006
  • The objective of this study was to evaluate the cytomorphologic features of histologically confirmed clear cell carcinoma of the ovary and to evaluate the applicability of scrape or fine-needle aspiration cytology in making an intraoperative diagnosis. We reviewed scrape or fine-needle aspiration cytology findings in tissues taken from 6 patients with clear cell carcinoma of the ovary. The cytologic diagnosis was based primarily on findings in alcohol-fixed, hematoxylin-eosin (H-E) stained smears. The formation of material resembling a basement membrane was a characteristic finding in these smears. This extracellular hyaline material was stained light pink with H-E and was frequently found within tumor cell clusters as well as in the background material. Multinucleated giant cells were found occasionally. Each tumor cell had an abundant, clear, or granular cytoplasm with a distinct cellular membrane. Scrape cytology is a simple and rapid supportive method and could be helpful in diagnosing clear cell carcinoma of the ovary, especially when marked artifacts appear in the frozen section.

전완골 분절의 전위 이식술 (Segmented Ulnar Transposition to Defect of Ipsilateral Radius in the Forearm)

  • 정덕환;한수홍;이재훈;권부경
    • Archives of Reconstructive Microsurgery
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    • 제16권2호
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    • pp.125-132
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    • 2007
  • Introduction: Ulna is nearly equal to radius in function and bony architecture and strength in forearm. But in lower extremity, fibula is 1/5 of tibia in anatomic and functional point so we can find fibula transposition is commonly used in defect of tibia. We cannot find other article about segmental forearm bone transposition in man. The purpose of this study was to report our clinical and functional result of undergoing segmented transposition of ipsilateral ulna with its own vascular supply in defect of radius in 6 cases. Material and method: From June 1994 to October 2007, 7 segmented bone transpositional grafts in forearm were performed in Kyung Hee Medical Center. The distribution of age was from 20 years old to 73 years old. There was male in 6 cases and female in 1 case. The causes of operation were giant cell tumor in 1 case and traumatic origin in 6 cases; it was nonunion in 2 cases and fracture with severe comminution in 4 cases. Ipsilaterally segmented ulna keeping its own vascular supply was transported to defect of radius in severe traumatic patients and one patient whose tumor in radius had been excised. Transported ulna was fixed to proximal and distal radius remnants by plate and screw. In one case with giant cell tumor, transported ulna was connected to radius across wrist joint as wrist joint fusion. Joint preserving procedures were performed in 6 cases with crushing injury of radius. Results: We could obtain solid bony union in all cases and good functional results. The disadvantage was relative shortening of forearm, but we could overcome this problem. Conclusion: We think that ipsilateral segmented ulna transposition keeping its own vascular supply to radius can be perfomed with one of procedures in cases with wide defect in radius.

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