• 대한두경부종양학회지
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• 제27권1호
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• pp.80-83
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• 2011

Paraganglioma is a relatively rare, generally benign and slow growing tumor arising from widely distributed paraganglionic tissue thought to originate from the neural crest. In the head and neck region, paraganglionic tissue is distributed in the superior and inferior paraganglia such as the carotid body, the vagal body, and the jugulotympanic region. Approximately 10% of patients with paraganglioma have a family history of such tumors. Multiple lesions can be found in 26% of patients with family history. It is important to distinguish between paraganglioma and atypical carcinoid tumor and medullary thyroid cancer. This can be done with histopathologic evaluation and immunohistochemical markers. Complete excision is recommended for the treatment of this tumor. Paraganglioma is particularly aggressive and rapid recurrence of paraganglioma is common after local resection. We present a case of malignant paraganglioma in the neck which recurred 2 months after local resection. We suppose that radiation therpay could be the last option for the treatment in this clinical setting.

• 대한두경부종양학회지
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• 제12권2호
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• pp.161-168
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• 1996

The neuorogenic tumor is known to be originated from neural crest, and the involved cells are Schwann cell, ganglion cell, and paraganglion cell. The Schwannoma, neurofibroma, and malignant schwannoma arise from the schwann cell, ganglioneuroma is from ganglion cell, and carotid body tumor and glomus tumor are originated from paraganglion cell. Authors reviewed thirty-eight patients of the neurogenic tumors in the head and neck, excluding intracranial tumor and Von-Recklinghausen disease, surgically treated at the Department of Surgery, Pusan Paik Hospital from January 1981 to May 1996. Of the 38 cases, 28 cases were schwannoma, 6 cases neurofibroma, 2 cases malignant schwannoma, and 2 cases paraganglioma. These tumors occurred at any age, but the majority of patients occurred in the fourth decade of life. There was female preponderance (M : F=1 : 1. 53) in sex ratio. The lateral cervical region was the most common distribution. 12 cases arose from the anterior triangle of neck, and 12 cases from the posterior triangle of neck. The major nerve origin of tumor could be identified in 30 cases (80%). 11 cases were treated by simple excision, and partial excision was 3 cases. Excision with parotidectomy 1 case, enucleation 11 cases, enucleation with parotidectomy 7 cases, radical neck dissection 1 cases, upper neck dissection 2 cases, suprahyoid dissection 1 case, Caldwell­Luc operation 1 case. The postoperative complications were hoarseness (2 cases), facial palsy (1 case), Homer syndrome (1 case), and hypoesthesia of tongue (1 case).

• 대한두경부종양학회지
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• 제36권2호
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• pp.51-53
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• 2020

Paraganglioma is a rare benign neuroendocrine tumor arising from the paraganglia of the autonomic nervous system. Paraganglioma occurs mainly in the carotid body, jugular foramen, and vagus nerve in the head and neck region. Herein, we report a case of paraganglioma of the submandibular region that has not been reported. This case highlights paraganglioma as a rare differential diagnosis for submandibular region tumors.

• 대한골관절종양학회지
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• 제11권1호
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• pp.94-99
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• 2005

부신경절종은, 신경외배엽 기원의 교감신경 신경내분비 세포로 이루어져 있는, 부신 이외의 부신경절에서 생긴 종양으로, 주로 갑상선, 목동맥체, 종격동, 폐, 십이지장, 대동맥 주변 부위와 후복막 부위에 잘 생긴다. 악성도는 조직학적인 진단에 의한 것이 아니라, 국소 림프절 재발과 원격 전이에 의하여 판별되며, 골 전이가 드물지만 전이가 일어나면 주로 두개골 기저, 척추에 생기며, 드물게 골반골, 대퇴골로 전이한다. 저자들은 대퇴부 피하층에 발생하여 혈관 기원성의 종양과 감별되었던 부신경절종과 조기 골 전이를 보인 후복막에 발생한 부신경 절종을 경험하여 문헌고찰과 함께 보고하고자 한다.

• 한국임상수의학회지
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• 제35권4호
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• pp.155-160
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• 2018

A 6-year-old intact female Shih-tzu dog was referred due to anorexia. Physical examination, complete blood count, serum chemical analysis, radiography, and ultrasonography were evaluated. Physical examination and hematological analysis showed normal findings. Abdominal radiographs and ultrasound revealed well-defined masses in the spleen. Other abdominal organs showed no significant abnormalities. Tissue samples taken via sono-guided fine needle aspiration of the splenic mass showed many bare nuclei, which were variable in size. Results of histopathological and immunohistochemical (IHC) analyses performed after splenectomy were consistent with paraganglioma. Based on these findings, we diagnosed this patient with a paraganglioma of splenic origin. Two months after splenectomy, abdominal ultrasonography revealed a new neoplastic lesion in the liver. The clients refused further management and the patient expired three months after initial diagnosis. Necropsy as well as histopathological and IHC examinations of other systemic organs including the liver, adrenal gland, kidney, brain, urinary bladder, lung, aortic body, carotid body, and pancreas were performed. The neoplastic tissue in the liver also demonstrated features of a paraganglioma, and there were no remarkable findings in all other organs.

• 한국의학물리학회지:의학물리
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• 제25권3호
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• pp.167-175
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• 2014

본 연구는 IMRT가 적용된 성문암 환자에 대하여 CBCT영상과 변형영상 정합기법을 이용하여 치료기간 동안 실제 환자에게 전달되는 선량 변화를 평가하고자 하였다. B-spline 알고리즘을 사용한 변형영상정합 시스템을 통해 치료 중 1주 간격으로 얻은 CBCT를 재구성하고 치료계획을 재계산하여 종양과 결정장기의 선량 분포를 비교하였다. 체중에 따른 체적변화는 3~5 주부터 평균 1.38~2.04 kg로 증가하였으며 체표면의 변화는 평균 2.1 mm로 감소하였다. 또한, 3주 이후의 경동맥에 전달된 선량은 계획되었던 값보다 최대 8.76%로 증가하였고, 갑상선샘은 26.4%로 감소하였다. 종양의 물리적의 평가인자인 PITV, TCI, rDHI, mDHI 그리고, CN은 치료 계획된 값보다 각각 평균 4.32%, 5.78%, 44.54%, 12.32% 그리고, 7.11%로 감소하였다. PTV에 대한 $D_{max}$는 평균 2.99% 증가하였고, $D_{mean}$, $V_{67.50}$, $D_{95}$는 각각 평균 1.52%, 5.78%, 11.94%로 감소하였다. 체중변화에 따른 체적의 변화가 없더라도 체형변화는 발생하였고, 좁은 여유마진을 가지는 IMRT는 이러한 변화에 민감하게 반응하였다. 성문암에 대한 IMRT 적용 시 환자의 체중변화를 관찰과 함께 변화를 기록하고 치료 중 변형영상정합 시스템을 이용하여 선량분포를 평가할 필요가 있다. 최종적으로 치료 중 실제 전달되는 선량평가는 적응형치료계획을 통하여 확인하고 정확한 선량전달이 필요하다고 사료된다.