• 제목/요약/키워드: Scalp mass

검색결과 59건 처리시간 0.022초

요추부에 발생한 경막외 유잉육종 - 증례 보고 - (Extraosseous Epidural Ewing's Sarcoma Arising in the Lumbar Area - A Case Report-)

  • 안면환;신덕섭;정광암;하정옥
    • 대한골관절종양학회지
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    • 제5권3호
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    • pp.183-189
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    • 1999
  • Ewing's sarcoma is an uncommon malignant neoplasm of the long bone and it has a poor prognosis due to its early metastasis and aggressive local spread. It is mostly found before the age of 30 and it is rare in extraskeletal sites. Extraskeletal Ewing's sarcoma has been reported to occur in various sites including the larynx, scalp, nasal fossa, neck, chest wall, lung, pelvis, perineum, arm, finger, leg and toe, but it is extremely rare as a primary epidural tumor of the spine. We experienced a case of extraosseous epidural Ewing's sarcoma arising in the lumbar spinal canal at L3-L5 level in a 9-year-old boy. Following total laminectomy from L3 to L5 with a lumbar vertebrae and mass excision, he received chemotherapy with complete remission.

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Technical and clinical aspects of cortisol as a biochemical marker of chronic stress

  • Lee, Do Yup;Kim, Eosu;Choi, Man Ho
    • BMB Reports
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    • 제48권4호
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    • pp.209-216
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    • 2015
  • Stress is now recognized as a universal premorbid factor associated with many risk factors of various chronic diseases. Acute stress may induce an individual's adaptive response to environmental demands. However, chronic, excessive stress causes cumulative negative impacts on health outcomes through "allostatic load". Thus, monitoring the quantified levels of long-term stress mediators would provide a timely opportunity for prevention or earlier intervention of stressrelated chronic illnesses. Although either acute or chronic stress could be quantified through measurement of changes in physiological parameters such as heart rate, blood pressure, and levels of various metabolic hormones, it is still elusive to interpret whether the changes in circulating levels of stress mediators such as cortisol can reflect the acute, chronic, or diurnal variations. Both serum and salivary cortisol levels reveal acute changes at a single point in time, but the overall long-term systemic cortisol exposure is difficult to evaluate due to circadian variations and its protein-binding capacity. Scalp hair has a fairy predictable growth rate of approximately 1 cm/month, and the most 1 cm segment approximates the last month's cortisol production as the mean value. The analysis of cortisol in hair is a highly promising technique for the retrospective assessment of chronic stress. [BMB Reports 2015; 48(4): 209-216]

Nodular scalp mass as the first presentation of pulmonary large cell neuroendocrine carcinoma: a case report

  • Hong Won Lee;Young Joong Hwang;Sung Gyun Jung;In Pyo Hong
    • 대한두개안면성형외과학회지
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    • 제24권5호
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    • pp.240-243
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    • 2023
  • Metastasis of lung cancer to the skin is uncommon, presenting in 0.22% to 12% of lung cancer patients, and it is extremely rare for skin metastasis to be the first clinical manifestation of lung cancer. In the few cases where skin metastasis has been reported as the first sign of lung cancer, the patients were typically heavy smokers or had preexisting respiratory diseases and symptoms. This prompted clinicians to consider skin metastasis of a pulmonary malignancy. Large cell neuroendocrine carcinoma (LCNEC) is a rare type of lung cancer that accounts for approximately 3% of lung cancers. LCNEC mainly metastasizes to visceral organs, such as the liver, bone, and brain, and it only shows metastasis to the skin in very rare cases. Herein, we report an unusual case of a metastatic skin lesion as the first sign of primary pulmonary LCNEC, in a 63-year-old woman with no pulmonary symptoms or personal history of smoking or pulmonary disease.

Spinal Cord Ependymoma Associated with Neurofibromatosis 1 : Case Report and Review of the Literature

  • Cheng, Hongwei;Shan, Ming;Feng, Chunguo;Wang, Xiaojie
    • Journal of Korean Neurosurgical Society
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    • 제55권1호
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    • pp.43-47
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    • 2014
  • Patients with neurofibromatosis 1 (NF1) are predisposed to develop central nervous system tumors, due to the loss of neurofibromin, an inactivator of proto-oncogene Ras. However, to our knowledge, only three cases of ependymomas with NF1 have been reported in the literature. The authors present a case of NF1 patient with a spinal cord ependymoma. She was referred for about half a year history of increasing numbness that progressed from her fingers to her entire body above the bellybutton. Magnetic resonance imaging revealed a relative-demarcated, heterogeneously enhanced mass lesion accompanied by perifocal edema in C5-7 level, a left-sided T11 spinous process heterogeneously enhanced mass in soft tissue, intervertebral disk hernia in L2-5 level, and widespread punctum enhancing lesion in her scalp and in T11-L5 level. The patient underwent C5-7 laminectomies and total excision of the tumor under operative microscope, and intraoperative ultrasonography and physiological monitoring were used during the surgery. Histopathologically, her tumor was found to be a ependymoma without malignant features (grade II in the World Health Organization classification). Therefore, no adjuvant therapy was applied. Following the operation, the patient showed an uneventful clinical recovery with no evidence of tumor recurrence after one year of follow-up.

측두부에 발생한 피부림프상피양 암종 증례보고 (A Case Report of Lymphoepithelioma-like Carcinoma on the Temple)

  • 오광진;이내호;양경무
    • 대한두개안면성형외과학회지
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    • 제9권1호
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    • pp.31-34
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    • 2008
  • Introduction: Lymphoepithelioma-like carcinoma of the skin (LELCS) is a rare cutaneous tumor of low grade malignancy and microscopically resembles lymphoepitheliomatous malignancies in the nasopharynx, palatine tonsils, salivary glands and uterine cervix. LELCS presents as scarlet-colored firm nodules or plaques on the face, scalp, or shoulder of middle-aged to elderly individuals. Material and Methods: A 72 year-old female had complained a papule like lesion with intermittent pruritis on the left temple for 2 years. But the lesion was changed to scarlet-colored firm nodule with ulceration. The mass was diagnosed as LELCS on the biopsy. And to confirm that the mass is not metastatic lymphoepithelioma-like carcinoma from other sites or direct tumor extension from the nasopharynx, selective radiographic and laboratory tests were done carefully. Results: Wide excision was performed with general endotracheal anesthesia. The tumor is composed of island of large epithelial cells surrounded by as dense infiltrate of lymphocytes. Immunohistochemical staining with cytokeratin and epithelial membrane antigen(EMA), the tumor cells were positive reaction for stain. And Epstein-Barr virus genome was not detected by in situ hybridization. So, the tumor was confirmed as LELCS. Conclusion: LELCS was described by Swanson at 1988, but has not been reported in the field of plastic surgery of Korea. We report a case of primary LELCS that occurred in the left temple with clinical characteristics, histologic features and references.

Combined treatment of surgery and sclerotherapy for sinus pericranii

  • Ryu, Jeong Yeop;Lee, Jong Ho;Lee, Joon Seok;Lee, Jeong Woo;Lee, Seok Jong;Lee, Jong Min;Lee, Sang Yub;Huh, Seung;Kim, Ji Yoon;Hwang, Sung Kyoo;Chung, Ho Yun
    • 대한두개안면성형외과학회지
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    • 제21권2호
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    • pp.109-113
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    • 2020
  • Sinus pericranii is a rare vascular anomaly characterized by abnormal venous communication between the inner and outer regions of the cranial cavity. Here, we report a case of sinus pericranii and venous malformations in the right periorbital region of a 2-year-old girl. Radiologic findings showed venous malformations in the right parietal region communicating with the superior sagittal sinus in the intracranial region. There were notable improvements following surgical resection for the abnormal venous lesions and several sclerotherapies. Presence of a bluish and pulsating mass on the scalp, which showed bruit on auscultation, may indicate sinus pericranii, which should be included in the differential diagnosis.

횡문근육종의 골전이가 동반된 워너증후군 1례 (A case of Werner Syndrome Complicated by Bone Metastasis of Rhabdomyosarcoma)

  • 송준환;선동신;김호;이윤희;홍용희;이동환
    • Journal of Genetic Medicine
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    • 제6권1호
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    • pp.91-94
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    • 2009
  • 저자들은 출생당시 특이소견 없었고, 유전질환의 가족력이 없는 20세 남자 환자에서 우측하지에 골전이가 동반된 횡문근 육종을 발견하고, 저신장, 탈모, 백내장, 치열이상, 골다공증, 갑상선기능저하증, 작은 손과 발, 사지는 가늘고 체간이 두터우며, 신체에 비해 큰 머리등 특이한 외모를 가진 워너증후군으로 진단한 1례를 경험하였기에 문헌 고찰과 함께 보고하고자 한다.

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악성 증식성 모낭 종양 - 증례 보고 - (Malignant Proliferating Trichilemmal Tumor - A Case Report -)

  • 홍기도;김재영;하성식;심재천;조혜제;최윤호
    • 대한골관절종양학회지
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    • 제15권1호
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    • pp.65-68
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    • 2009
  • 증식성 모낭 종양은 모낭 말단부위의 외근모초에서 기원하는 드문 종양이다. 악성 변화는 드물지만 갑작스러운 크기의 증가, 침윤성 성장 및 두피 이외에서 종양의 발생 등은 악성 증식성 모낭 종양을 시사한다. 병리조직학적으로 핵의 이형성, 다형성 및 유사분열 소견은 악성증식성 모낭 종양의 특징이다. 악성 증식성 모낭 종양은 재발 및 전이가 보고되고 있어 정상조직을 포함한 충분한 절제와 추적관찰이 요구된다. 53세 남자 환자의 우측 제 5수지 원위 지골에 7년전 발생한 종양을 중위 지이하 절제술 후 병리조직검사상 악성 증식성 모낭 종양으로 진단되었고, 환자가 외래로 더 이상 방문하지 않아 재발과 전이를 확인할 수 없었다.

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소아 대장에서 발생한 전이성 반지세포암 1예 (A Case of Metastatic Signet Ring Cell Carcinoma of the Colon in a Child)

  • 오대성;한경희;신지연;심정옥;박지숙;양혜란;고재성;신희영;안효섭;박귀원;강경훈;천정은;김우선;서정기
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제10권1호
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    • pp.76-80
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    • 2007
  • 소아암에서 장관계 악성 종양 특히, 대장암은 극히 드문 질환이다. 그러나, 대장은 소아 장관계 상피세포암이 가장 호발하는 부위이며, 반지세포암은 성인과는 달리 소아 대장암 중에서 가장 흔한 조직형태 중 하나이다. 국내에서는 소아 대장에서 발생한 반지세포암에 대한 보고는 아직 없었다. 반지세포암은 점액이 세포내에 풍부하고 핵이 한쪽으로 치우쳐 있는 특징적 고리모양의 암 세포가 전체 암 세포의 50% 이상을 차지하는 조직 소견으로 진단된다. 저자들은 복통, 체중감소, 요통, 좌측 대퇴부 통증, 혈변으로 내원한 11세 남아에서 내시경 조직검사 소견으로 확진된 복강내 침습, 혈액 및 림프성 전이가 진행된 소아 대장에서의 전이성반지세포암을 경험하였기에 보고하는 바이다.

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