- Robotic enucleation of a pancreatic uncinate neuroendocrine tumor – a unique parenchyma-saving strategy for uncinate tumors
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Chin KM, Goh BK
- KMID: 2471197
- Ann Hepatobiliary Pancreat Surg.
- 2020 Feb;24(1):97-103.
- doi: 10.14701/ahbps.2020.24.1.97
Pancreatic neuroendocrine tumors (PNET) comprise up to 10% of all pancreatic solid tumors. There has been much interest in recent years with regards to the role of limited resection and... -
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- Validation of the 8th AJCC Cancer Staging System for Pancreas Neuroendocrine Tumors Using Korean Nationwide Surgery Database
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You Y, Jang JY, Kim SC, Yoon YS, Park JS, Cho CK, Park SJ, Yang JD, Lee WJ, Hong TH, Ahn KS, Jeong CY, Lee HK, Lee SE, Roh YH, Kim HJ, Kim H, Han IW
- KMID: 2460612
- Cancer Res Treat.
- 2019 Oct;51(4):1639-1652.
- doi: 10.4143/crt.2019.023
PURPOSE: The 8th edition of the American Joint Committee on Cancer (AJCC) staging system for pancreatic neuroendocrine tumor (PNET) included several significant changes. We aim to evaluate this staging system... -
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- Ewing Sarcoma
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Ju HY
- KMID: 2449228
- Clin Pediatr Hematol Oncol.
- 2019 Apr;26(1):27-34.
- doi: 10.15264/cpho.2019.26.1.27
Ewing sarcoma is the second most frequently occurring malignant tumor of the bone and soft tissue in adolescents and young adults. Genetically, Ewing sarcoma is characterized by balanced chromosomal translocation... -
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- Recent Updates in the Management of Advanced Pancreatic Neuroendocrine Tumors
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Cho CM
- KMID: 2442078
- Korean J Gastroenterol.
- 2019 Mar;73(3):124-131.
- doi: 10.4166/kjg.2019.73.3.124
Pancreatic neuroendocrine tumors (pNETs) are rare neoplasms arising from the pancreatic islet of Langerhans and can be functioning or non-functioning based on the clinical symptoms caused by hormonal secretions. PNETs... -
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- A Case of Long-term Survival in a Patient with Primary Primitive Neuroectodermal Tumor of the Lung
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Kang LH, Kim HJ, Jang JH, Kim JH, Choi KU, Jeon D
- KMID: 2430745
- Kosin Med J.
- 2018 Dec;33(2):263-270.
- doi: 10.7180/kmj.2018.33.2.263
Primitive neuroectodermal tumor (PNET) arising primarily in the lung is an extremely rare and aggressive malignancy with poor chances of patient survival. We present a case of long-term survival by... -
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- Thyroid dysfunction in patients with childhood-onset medulloblastoma or primitive neuroectodermal tumor
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Jin SY, Choi JY, Park KD, Kang HJ, Shin HY, Phi JH, Kim SK, Wang KC, Kim IH, Lee YA, Shin CH, Yang SW
- KMID: 2417765
- Ann Pediatr Endocrinol Metab.
- 2018 Jun;23(2):88-93.
- doi: 10.6065/apem.2018.23.2.88
PURPOSE: We investigated the clinical characteristics of patients who developed thyroid dysfunction and evaluated the risk factors for hypothyroidism following radiotherapy and chemotherapy in pediatric patients with medulloblastoma or primitive... -
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- Successful Surgical Treatment of a Recurrent Esophageal Malignant Gastrointestinal Neuroectodermal Tumor
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Song SH, Shin JH, Ryu HJ, Kim DJ, Park SY
- KMID: 2409700
- Korean J Thorac Cardiovasc Surg.
- 2018 Apr;51(2):142-145.
- doi: 10.5090/kjtcs.2018.51.2.142
Malignant gastrointestinal neuroectodermal tumor (GNET) is a very rare disease entity, especially in the esophagus. The diagnosis of GNET is based on histologic, immunohistochemical, and genetic findings. The choice of... -
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- Therapy of Pancreatic Neuroendocrine Tumors: Fine Needle Intervention including Ethanol and Radiofrequency Ablation
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Lakhtakia
- KMID: 2398305
- Clin Endosc.
- 2017 Nov;50(6):546-551.
- doi: 10.5946/ce.2017.167
Pancreatic neuroendocrine tumors (PNETs) are increasingly being detected, though usually as incidental findings. Majority of the PNETs are non-functional and surgical resection is the standard of care for most of... -
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- Diagnosis of Pancreatic Neuroendocrine Tumors
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Lee DW, Kim MK, Kim HG
- KMID: 2398304
- Clin Endosc.
- 2017 Nov;50(6):537-545.
- doi: 10.5946/ce.2017.131
Pancreatic neuroendocrine tumors (PNETs) are relatively rare; however, the incidence has increased over the last few decades. They are classified as functional or non-functional tumors according to the presence of... -
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- Pediatric Ewing's Sarcoma/Primitive Neuroectodermal Tumor (ES/PNET) Developed in the Small Intestine: A Case Report
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Kim YS, Moon HM, Lee KS, Park YS, Kim HY, Kim JY, Cho JM, Choi HS
- KMID: 2396021
- Clin Pediatr Hematol Oncol.
- 2017 Oct;24(2):162-168.
- doi: 10.15264/cpho.2017.24.2.162
Ewing sarcoma/primitive neuroectodermal tumors (ES/PNET) are a group of malignant tumors with varying degrees of neuroectodermal differentiation. Although it may develop in any organs, ES/PNET originating from small intestine is... -
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- Renal Tumors in Children
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Lee SW
- KMID: 2379347
- Clin Pediatr Hematol Oncol.
- 2017 Apr;24(1):21-36.
- doi: 10.15264/cpho.2017.24.1.21
Pediatric renal tumors represent a diverse group, which include Wilms' tumor (WT), renal cell carcinoma (RCC), clear cell sarcoma of the kidney (CCSK), congenital mesoblastic nephroma, malignant rhabdoid tumor of... -
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- Clinical role of contrast-enhanced harmonic endoscopic ultrasound in differentiating pancreatic solid lesions
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Shim CS, Lee TY, Cheon YK
- KMID: 2358134
- Gastrointest Interv.
- 2016 Oct;5(3):177-182.
- doi: 10.18528/gii.2016.5.3.177
Accurate diagnosis of pancreatic solid lesions is often difficult using conventional imaging modalities. With the recent introduction of contrast-enhanced harmonic endoscopic ultrasound (CEH-EUS), it is now possible to evaluate the... -
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- Optimal Treatment of Advanced Pancreatic Neuroendocrine Tumor
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Kim YS, Cho JH
- KMID: 2448526
- Korean J Pancreas Biliary Tract.
- 2016 Jul;21(3):128-137.
- doi: 10.15279/kpba.2016.21.3.128
Pancreatic neuroendocrine tumors (pNETs) are diverse diseases with different prognosis. Among available various therapeutic options, curative resection should be considered for localized tumors and in some selected cases of metastatic... -
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- Sellar-Suprasellar Extraventricular Choroid Plexus Papilloma : A Case Report and Review of the Literature
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Keskin F, Erdi F, Kaya B, Toy H
- KMID: 2152919
- J Korean Neurosurg Soc.
- 2016 Jan;59(1):58-61.
- doi: 10.3340/jkns.2016.59.1.58
Choroid plexus papillomas (CPPs) are relatively rare neuroectodermal tumors that develop from choroid plexus epithelial cells and are usually restricted to the ventricles. Extraventricular CPPs are very unusual and can... -
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- Isolated Supratentorial Intraventricular Recurrence of Medulloblastoma
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Abode-Iyamah KO, Winslow N, Flouty O, Kirby P
- KMID: 2151160
- J Korean Neurosurg Soc.
- 2015 Dec;58(6):557-559.
- doi: 10.3340/jkns.2015.58.6.557
Medulloblastoma is a common pediatric tumor typically diagnosed before the age of fifteen. Initial therapy includes surgical resection and radiation of the entire neuro-axis. Recurrence is common and typically occurs... -
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- Unusual Malignant Solid Neoplasms of the Kidney: Cross-Sectional Imaging Findings
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Karaosmanoglu AD, Onur MR, Shirkhoda , Ozmen M, Hahn PF
- KMID: 2155559
- Korean J Radiol.
- 2015 Aug;16(4):853-859.
- doi: 10.3348/kjr.2015.16.4.853
Malignant kidney neoplasms are the most frequently encountered solid kidney masses. Although renal cell carcinoma is the major renal malignancy, other solid malignant renal masses should be considered in the... -
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- Imaging Features of Primary Tumors and Metastatic Patterns of the Extraskeletal Ewing Sarcoma Family of Tumors in Adults: A 17-Year Experience at a Single Institution
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Huh J, Kim KW, Park SJ, Kim HJ, Lee JS, Ha HK, Tirumani S, Ramaiya NH
- KMID: 2155551
- Korean J Radiol.
- 2015 Aug;16(4):783-790.
- doi: 10.3348/kjr.2015.16.4.783
OBJECTIVE: To comprehensively analyze the spectrum of imaging features of the primary tumors and metastatic patterns of the Extraskeletal Ewing sarcoma family of tumors (EES) in adults. MATERIALS AND METHODS: We... -
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- A Case of Primary Cutaneous CD30+ Anaplastic Large Cell Lymphoma, Small Cell Variant
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Min J, Kim HS, Hwang SH, Lee HJ, Nam JH, Jung HJ, Park JH, Lee GY, Kim WS
- KMID: 2301509
- Korean J Dermatol.
- 2015 May;53(4):304-309.
Primary cutaneous anaplastic large cell lymphoma (PCALCL) is a rare cutaneous T-cell lymphoma. Most cases are composed of large anaplastic cells. However, it presents a wide spectrum of histologic patterns.... -
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- Giant malignant insulinoma
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Karavias D, Habeos I, Maroulis I, Kalogeropoulou C, Tsamandas , Chaveles I, Karavias D
- KMID: 2166998
- Ann Surg Treat Res.
- 2015 May;88(5):289-293.
- doi: 10.4174/astr.2015.88.5.289
Insulinomas are the most common pancreatic neuroendocrine tumors. Most insulinomas are benign, small, intrapancreatic solid tumors and only large tumors have a tendency for malignancy. Most patients present with symptoms... -
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- Utility of Transmission Electron Microscopy in Small Round Cell Tumors
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Kim NR, Ha SY, Cho HY
- KMID: 2381362
- J Pathol Transl Med.
- 2015 Mar;49(2):93-101.
- doi: 10.4132/jptm.2015.01.30
Small round cell tumors (SRCTs) are a heterogeneous group of neoplasms composed of small, primitive, and undifferentiated cells sharing similar histology under light microscopy. SRCTs include Ewing sarcoma/peripheral neuroectodermal tumor... -
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