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Showing 1 to 12 of 1724 entries
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Central Myxoma / Myxofibroma of the Jaws: A Clinico-Epidemiologic Review.

Iranian journal of otorhinolaryngology

Rowland A, Benjamin F, Athanasius-Chukwudi O, Uchenna-Kevin O, Modupeola-Omotara S.
PMID: 28229061
Iran J Otorhinolaryngol. 2017 Jan;29(90):35-42.

INTRODUCTION: Myxomas are a group of benign rare tumors of connective-tissue origin that occur in both hard (central) and soft tissues of the body. The aim of this study is to highlight our experience in the management of central...

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Rowland A, Benjamin F, Athanasius-Chukwudi O, et al. Central Myxoma / Myxofibroma of the Jaws: A Clinico-Epidemiologic Review. Iran J Otorhinolaryngol. 2017;29(90):35-42
Rowland, A., Benjamin, F., Athanasius-Chukwudi, O., Uchenna-Kevin, O., & Modupeola-Omotara, S. (2017). Central Myxoma / Myxofibroma of the Jaws: A Clinico-Epidemiologic Review. Iranian journal of otorhinolaryngology, 29(90), 35-42.
Rowland, Agbara, et al. "Central Myxoma / Myxofibroma of the Jaws: A Clinico-Epidemiologic Review." Iranian journal of otorhinolaryngology vol. 29,90 (2017): 35-42.
Rowland A, Benjamin F, Athanasius-Chukwudi O, Uchenna-Kevin O, Modupeola-Omotara S. Central Myxoma / Myxofibroma of the Jaws: A Clinico-Epidemiologic Review. Iran J Otorhinolaryngol. 2017 Jan;29(90):35-42. PMID: 28229061; PMCID: PMC5307303.
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Gastrointestinal stromal tumor of the vermiform appendix mimicking Meckel's diverticulum: Case report with literature review.

International journal of surgery case reports

Chun JM, Lim KH.
PMID: 26895113
Int J Surg Case Rep. 2016;21:20-2. doi: 10.1016/j.ijscr.2016.02.010. Epub 2016 Feb 08.

INTRODUCTION: Gastrointestinal stromal tumors (GISTs) of the appendix are extremely rare. To date, only 15 cases have been reported in the English literature. Here, we present a new case of an appendiceal GIST with appendicitis.PRESENTATION OF CASE: A 68-year-old...

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Chun JM, Lim KH. Gastrointestinal stromal tumor of the vermiform appendix mimicking Meckel's diverticulum: Case report with literature review. Int J Surg Case Rep. 2016;21:20-2doi: 10.1016/j.ijscr.2016.02.010.
Chun, J. M., & Lim, K. H. (2016). Gastrointestinal stromal tumor of the vermiform appendix mimicking Meckel's diverticulum: Case report with literature review. International journal of surgery case reports, 2120-2. https://doi.org/10.1016/j.ijscr.2016.02.010
Chun, Jae Min, and Lim, Kyoung Hoon. "Gastrointestinal stromal tumor of the vermiform appendix mimicking Meckel's diverticulum: Case report with literature review." International journal of surgery case reports vol. 21 (2016): 20-2. doi: https://doi.org/10.1016/j.ijscr.2016.02.010
Chun JM, Lim KH. Gastrointestinal stromal tumor of the vermiform appendix mimicking Meckel's diverticulum: Case report with literature review. Int J Surg Case Rep. 2016;21:20-2. doi: 10.1016/j.ijscr.2016.02.010. Epub 2016 Feb 08. PMID: 26895113; PMCID: PMC4802133.
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Analysis of non-squamous vulvar cancer cases: A 21-year experience in a single center.

Turkish journal of obstetrics and gynecology

Akdağ Cırık D, Kalyoncu R, Üreyen I, Taşçı T, Boran N, Özfuttu A, Turan T, Tulunay G.
PMID: 28913011
Turk J Obstet Gynecol. 2014 Sep;11(3):165-169. doi: 10.4274/tjod.83436. Epub 2014 Sep 15.

OBJECTIVE: To evaluate the patients with non-squamous cell type of vulvar cancer who were treated in our clinic within 21 years.MATERIALS AND METHODS: We assessed the data of 14 patients who were treated for non-squamous cancer of the vulva...

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Akdağ Cırık D, Kalyoncu R, Üreyen I, et al. Analysis of non-squamous vulvar cancer cases: A 21-year experience in a single center. Turk J Obstet Gynecol. 2014;11(3):165-169doi: 10.4274/tjod.83436.
Akdağ Cırık, D., Kalyoncu, R., Üreyen, I., Taşçı, T., Boran, N., Özfuttu, A., Turan, T., & Tulunay, G. (2014). Analysis of non-squamous vulvar cancer cases: A 21-year experience in a single center. Turkish journal of obstetrics and gynecology, 11(3), 165-169. https://doi.org/10.4274/tjod.83436
Akdağ Cırık, Derya, et al. "Analysis of non-squamous vulvar cancer cases: A 21-year experience in a single center." Turkish journal of obstetrics and gynecology vol. 11,3 (2014): 165-169. doi: https://doi.org/10.4274/tjod.83436
Akdağ Cırık D, Kalyoncu R, Üreyen I, Taşçı T, Boran N, Özfuttu A, Turan T, Tulunay G. Analysis of non-squamous vulvar cancer cases: A 21-year experience in a single center. Turk J Obstet Gynecol. 2014 Sep;11(3):165-169. doi: 10.4274/tjod.83436. Epub 2014 Sep 15. PMID: 28913011; PMCID: PMC5558328.
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Paraganglioma of the organ of Zuckerkandl associated with a somatic .

Oncology letters

Abdullah AE, Guerin C, Imperiale A, Barlier A, Battini S, Pertuit M, Roche P, Essamet W, Vaisse B, Pacak K, Sebag F, Taïeb D.
PMID: 28454217
Oncol Lett. 2017 Mar;13(3):1083-1086. doi: 10.3892/ol.2017.5599. Epub 2017 Jan 12.

Paragangliomas of the organ of Zuckerkandl (OZ-PGL) are rare tumors that, in >70% of cases, occur in association with succinate dehydrogenase complex iron sulfur subunit B (

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Abdullah AE, Guerin C, Imperiale A, et al. Paraganglioma of the organ of Zuckerkandl associated with a somatic . Oncol Lett. 2017;13(3):1083-1086doi: 10.3892/ol.2017.5599.
Abdullah, A. E., Guerin, C., Imperiale, A., Barlier, A., Battini, S., Pertuit, M., Roche, P., Essamet, W., Vaisse, B., Pacak, K., Sebag, F., & Taïeb, D. (2017). Paraganglioma of the organ of Zuckerkandl associated with a somatic . Oncology letters, 13(3), 1083-1086. https://doi.org/10.3892/ol.2017.5599
Abdullah, Ahmad Esmaeel, et al. "Paraganglioma of the organ of Zuckerkandl associated with a somatic ." Oncology letters vol. 13,3 (2017): 1083-1086. doi: https://doi.org/10.3892/ol.2017.5599
Abdullah AE, Guerin C, Imperiale A, Barlier A, Battini S, Pertuit M, Roche P, Essamet W, Vaisse B, Pacak K, Sebag F, Taïeb D. Paraganglioma of the organ of Zuckerkandl associated with a somatic . Oncol Lett. 2017 Mar;13(3):1083-1086. doi: 10.3892/ol.2017.5599. Epub 2017 Jan 12. PMID: 28454217; PMCID: PMC5403169.
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Variegated Colors of Pediatric Glioblastoma Multiforme: What to Expect?.

Rare tumors

Immanuel V, Kingsley PA, Negi P, Isaacs R, Grewal SS.
PMID: 28975017
Rare Tumors. 2017 Aug 29;9(2):6552. doi: 10.4081/rt.2017.6552. eCollection 2017 Jul 03.

Malignant gliomas account for 35-45% of primary brain tumors; among these glioblastoma multiforme (GBM) is the most common adult brain tumor constituting approximately 85%. Its incidence is quite less in the pediatric population and treatment of these patients is...

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Immanuel V, Kingsley PA, Negi P, et al. Variegated Colors of Pediatric Glioblastoma Multiforme: What to Expect?. Rare Tumors. 2017;9(2):6552doi: 10.4081/rt.2017.6552.
Immanuel, V., Kingsley, P. A., Negi, P., Isaacs, R., & Grewal, S. S. (2017). Variegated Colors of Pediatric Glioblastoma Multiforme: What to Expect?. Rare tumors, 9(2), 6552. https://doi.org/10.4081/rt.2017.6552
Immanuel, Vivek, et al. "Variegated Colors of Pediatric Glioblastoma Multiforme: What to Expect?." Rare tumors vol. 9,2 (2017): 6552. doi: https://doi.org/10.4081/rt.2017.6552
Immanuel V, Kingsley PA, Negi P, Isaacs R, Grewal SS. Variegated Colors of Pediatric Glioblastoma Multiforme: What to Expect?. Rare Tumors. 2017 Aug 29;9(2):6552. doi: 10.4081/rt.2017.6552. eCollection 2017 Jul 03. PMID: 28975017; PMCID: PMC5617915.
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A Case of Neuroendocrine Carcinoma Developing from the Broad Ligament of the Uterus.

Rare tumors

Itonaga Y, Nishida M, Matsumoto H, Nasu K, Narahara H.
PMID: 28975020
Rare Tumors. 2017 Jul 03;9(2):6958. doi: 10.4081/rt.2017.6958. eCollection 2017 Jul 03.

Neuroendocrine carcinoma (NEC), also called small cell carcinoma or large cell carcinoma, is a rare and aggressive tumor that develops mainly in the lung and intestine. More rarely, NEC develops in gynecologic organs, with poor prognoses. We experienced a...

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Itonaga Y, Nishida M, Matsumoto H, et al. A Case of Neuroendocrine Carcinoma Developing from the Broad Ligament of the Uterus. Rare Tumors. 2017;9(2):6958doi: 10.4081/rt.2017.6958.
Itonaga, Y., Nishida, M., Matsumoto, H., Nasu, K., & Narahara, H. (2017). A Case of Neuroendocrine Carcinoma Developing from the Broad Ligament of the Uterus. Rare tumors, 9(2), 6958. https://doi.org/10.4081/rt.2017.6958
Itonaga, Yui, et al. "A Case of Neuroendocrine Carcinoma Developing from the Broad Ligament of the Uterus." Rare tumors vol. 9,2 (2017): 6958. doi: https://doi.org/10.4081/rt.2017.6958
Itonaga Y, Nishida M, Matsumoto H, Nasu K, Narahara H. A Case of Neuroendocrine Carcinoma Developing from the Broad Ligament of the Uterus. Rare Tumors. 2017 Jul 03;9(2):6958. doi: 10.4081/rt.2017.6958. eCollection 2017 Jul 03. PMID: 28975020; PMCID: PMC5617910.
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Thoracic psammomatous spinal meningioma with osseous metaplasia: A very rare case report.

Asian journal of neurosurgery

Prakash A, Mishra S, Tyagi R, Attri PC, Bhatnagar A, Kansal S.
PMID: 28484549
Asian J Neurosurg. 2017 Apr-Jun;12(2):270-272. doi: 10.4103/1793-5482.150222.

Thoracic spinal psammomatous meningioma is a rare subtype of meningioma. Among diverse types of mesenchymal differentiation, osseous metaplasia is found to be still rarer. We are presenting a new case of thoracic psammomatous spinal meningioma with osseous metaplasia in...

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Prakash A, Mishra S, Tyagi R, et al. Thoracic psammomatous spinal meningioma with osseous metaplasia: A very rare case report. Asian J Neurosurg. 2017;12(2):270-272doi: 10.4103/1793-5482.150222.
Prakash, A., Mishra, S., Tyagi, R., Attri, P. C., Bhatnagar, A., & Kansal, S. (2017). Thoracic psammomatous spinal meningioma with osseous metaplasia: A very rare case report. Asian journal of neurosurgery, 12(2), 270-272. https://doi.org/10.4103/1793-5482.150222
Prakash, Akhil, et al. "Thoracic psammomatous spinal meningioma with osseous metaplasia: A very rare case report." Asian journal of neurosurgery vol. 12,2 (2017): 270-272. doi: https://doi.org/10.4103/1793-5482.150222
Prakash A, Mishra S, Tyagi R, Attri PC, Bhatnagar A, Kansal S. Thoracic psammomatous spinal meningioma with osseous metaplasia: A very rare case report. Asian J Neurosurg. 2017 Apr-Jun;12(2):270-272. doi: 10.4103/1793-5482.150222. PMID: 28484549; PMCID: PMC5409385.
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Paragangliomas: À Propos of Two Cases. Diagnostics and Treatment.

Polish journal of radiology

Pałasz P, Adamski Ł, Studniarek M.
PMID: 26405465
Pol J Radiol. 2015 Aug 01;80:411-6. doi: 10.12659/PJR.894702. eCollection 2015.

BACKGROUND: Paraganglioma develops from cells of the parasympathetic and sympathetic system. It usually manifests as a slow-growing and painless mass. Peragangliomas may be hereditary, benign or malignant, unilateral or bilateral tumors. They are well vascularized. In most cases, paraganglioma...

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Pałasz P, Adamski Ł, Studniarek M. Paragangliomas: À Propos of Two Cases. Diagnostics and Treatment. Pol J Radiol. 2015;80:411-6doi: 10.12659/PJR.894702.
Pałasz, P., Adamski, �. �., & Studniarek, M. (2015). Paragangliomas: À Propos of Two Cases. Diagnostics and Treatment. Polish journal of radiology, 80411-6. https://doi.org/10.12659/PJR.894702
Pałasz, Paulina, et al. "Paragangliomas: À Propos of Two Cases. Diagnostics and Treatment." Polish journal of radiology vol. 80 (2015): 411-6. doi: https://doi.org/10.12659/PJR.894702
Pałasz P, Adamski Ł, Studniarek M. Paragangliomas: À Propos of Two Cases. Diagnostics and Treatment. Pol J Radiol. 2015 Aug 01;80:411-6. doi: 10.12659/PJR.894702. eCollection 2015. PMID: 26405465; PMCID: PMC4562611.
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Primitive neuroectodermal tumor in the spinal canal: A case report.

Oncology letters

Meng XT, He SS.
PMID: 25789071
Oncol Lett. 2015 Apr;9(4):1934-1936. doi: 10.3892/ol.2015.2907. Epub 2015 Jan 27.

Primitive neuroectodermal tumors (PNETs) are rare tumors of uncertain histogenesis that occur predominantly in children and young adults. The current study reports a case of PNET in a 60-year-old female, which presented clinically as an intraspinal tumor, causing symptoms...

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Meng XT, He SS. Primitive neuroectodermal tumor in the spinal canal: A case report. Oncol Lett. 2015;9(4):1934-1936doi: 10.3892/ol.2015.2907.
Meng, X. T., & He, S. S. (2015). Primitive neuroectodermal tumor in the spinal canal: A case report. Oncology letters, 9(4), 1934-1936. https://doi.org/10.3892/ol.2015.2907
Meng, Xiao-Tong, and He, Shi-Sheng. "Primitive neuroectodermal tumor in the spinal canal: A case report." Oncology letters vol. 9,4 (2015): 1934-1936. doi: https://doi.org/10.3892/ol.2015.2907
Meng XT, He SS. Primitive neuroectodermal tumor in the spinal canal: A case report. Oncol Lett. 2015 Apr;9(4):1934-1936. doi: 10.3892/ol.2015.2907. Epub 2015 Jan 27. PMID: 25789071; PMCID: PMC4356409.
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Breast Metastasis from Medullary Thyroid Carcinoma in a Male Patient: Case Report and Review of the Literature.

Rare tumors

Mandanas S, Margaritidou E, Christoforidou V, Karoglou E, Geranou C, Chrisoulidou A, Boudina M, Georgopoulos K, Pazaitou-Panayiotou K.
PMID: 26266011
Rare Tumors. 2015 May 18;7(2):5765. doi: 10.4081/rt.2015.5765. eCollection 2015 May 05.

Medullary thyroid carcinoma (MTC) is a rare malignancy that may metastasize to liver, lungs and bones. Breast is an unusual metastatic site for MTC and only 20 female cases have been reported in the literature. We present a male...

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Mandanas S, Margaritidou E, Christoforidou V, et al. Breast Metastasis from Medullary Thyroid Carcinoma in a Male Patient: Case Report and Review of the Literature. Rare Tumors. 2015;7(2):5765doi: 10.4081/rt.2015.5765.
Mandanas, S., Margaritidou, E., Christoforidou, V., Karoglou, E., Geranou, C., Chrisoulidou, A., Boudina, M., Georgopoulos, K., & Pazaitou-Panayiotou, K. (2015). Breast Metastasis from Medullary Thyroid Carcinoma in a Male Patient: Case Report and Review of the Literature. Rare tumors, 7(2), 5765. https://doi.org/10.4081/rt.2015.5765
Mandanas, Stylianos, et al. "Breast Metastasis from Medullary Thyroid Carcinoma in a Male Patient: Case Report and Review of the Literature." Rare tumors vol. 7,2 (2015): 5765. doi: https://doi.org/10.4081/rt.2015.5765
Mandanas S, Margaritidou E, Christoforidou V, Karoglou E, Geranou C, Chrisoulidou A, Boudina M, Georgopoulos K, Pazaitou-Panayiotou K. Breast Metastasis from Medullary Thyroid Carcinoma in a Male Patient: Case Report and Review of the Literature. Rare Tumors. 2015 May 18;7(2):5765. doi: 10.4081/rt.2015.5765. eCollection 2015 May 05. PMID: 26266011; PMCID: PMC4508642.
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Digital Papillary Adenocarcinoma: Presentation, Natural History and Management.

Rare tumors

Carter K, Yao JJ, Melton SD, Lopez J, Huerta S.
PMID: 26266016
Rare Tumors. 2015 Jun 25;7(2):5867. doi: 10.4081/rt.2015.5867. eCollection 2015 May 05.

Digital papillary adenocarcinoma (DPA) is a rare malignant tumor of the sweat glands that often presents as a solitary painless mass on the digits of the hands or feet. We present a rare case of DPA on the ankle...

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Carter K, Yao JJ, Melton SD, et al. Digital Papillary Adenocarcinoma: Presentation, Natural History and Management. Rare Tumors. 2015;7(2):5867doi: 10.4081/rt.2015.5867.
Carter, K., Yao, J. J., Melton, S. D., Lopez, J., & Huerta, S. (2015). Digital Papillary Adenocarcinoma: Presentation, Natural History and Management. Rare tumors, 7(2), 5867. https://doi.org/10.4081/rt.2015.5867
Carter, Kristen, et al. "Digital Papillary Adenocarcinoma: Presentation, Natural History and Management." Rare tumors vol. 7,2 (2015): 5867. doi: https://doi.org/10.4081/rt.2015.5867
Carter K, Yao JJ, Melton SD, Lopez J, Huerta S. Digital Papillary Adenocarcinoma: Presentation, Natural History and Management. Rare Tumors. 2015 Jun 25;7(2):5867. doi: 10.4081/rt.2015.5867. eCollection 2015 May 05. PMID: 26266016; PMCID: PMC4508647.
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Trabecular Variant of Juvenile Aggressive Ossifying Fibroma.

Rare tumors

Rahman T, Hashmi GS, Ansari H.
PMID: 26266018
Rare Tumors. 2015 Jun 25;7(2):5890. doi: 10.4081/rt.2015.5890. eCollection 2015 May 05.

Juvenile aggressive ossifying fibroma (JAOF) is an uncommon benign lesion which is distinctly aggressive in behavior with high tendency for recurrence. It appears in early age and in 79% of patients is diagnosed before 15. It has two histological...

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Rahman T, Hashmi GS, Ansari H. Trabecular Variant of Juvenile Aggressive Ossifying Fibroma. Rare Tumors. 2015;7(2):5890doi: 10.4081/rt.2015.5890.
Rahman, T., Hashmi, G. S., & Ansari, H. (2015). Trabecular Variant of Juvenile Aggressive Ossifying Fibroma. Rare tumors, 7(2), 5890. https://doi.org/10.4081/rt.2015.5890
Rahman, Tabishur, et al. "Trabecular Variant of Juvenile Aggressive Ossifying Fibroma." Rare tumors vol. 7,2 (2015): 5890. doi: https://doi.org/10.4081/rt.2015.5890
Rahman T, Hashmi GS, Ansari H. Trabecular Variant of Juvenile Aggressive Ossifying Fibroma. Rare Tumors. 2015 Jun 25;7(2):5890. doi: 10.4081/rt.2015.5890. eCollection 2015 May 05. PMID: 26266018; PMCID: PMC4508649.
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Showing 1 to 12 of 1724 entries