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Showing 1 to 12 of 127 entries
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Intraoperative near-infrared fluorescence imaging of a paraganglioma using methylene blue: A case report.

International journal of surgery case reports

Tummers QR, Boonstra MC, Frangioni JV, van de Velde CJ, Vahrmeijer AL, Bonsing BA.
PMID: 25541370
Int J Surg Case Rep. 2015;6:150-3. doi: 10.1016/j.ijscr.2014.12.002. Epub 2014 Dec 05.

INTRODUCTION: Intraoperative identification of tumors can be challenging. Near-infrared (NIR) fluorescence imaging is an innovative technique that can assist in intraoperative identification of tumors, which may otherwise be undetectable.PRESENTATION OF CASE: A 19-year-old patient with symptoms, normetanephrine levels and...

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Tummers QR, Boonstra MC, Frangioni JV, et al. Intraoperative near-infrared fluorescence imaging of a paraganglioma using methylene blue: A case report. Int J Surg Case Rep. 2014;6:150-3doi: 10.1016/j.ijscr.2014.12.002.
Tummers, Q. R., Boonstra, M. C., Frangioni, J. V., van de Velde, C. J., Vahrmeijer, A. L., & Bonsing, B. A. (2015). Intraoperative near-infrared fluorescence imaging of a paraganglioma using methylene blue: A case report. International journal of surgery case reports, 6150-3. https://doi.org/10.1016/j.ijscr.2014.12.002
Tummers, Quirijn R J G, et al. "Intraoperative near-infrared fluorescence imaging of a paraganglioma using methylene blue: A case report." International journal of surgery case reports vol. 6 (2015): 150-3. doi: https://doi.org/10.1016/j.ijscr.2014.12.002
Tummers QR, Boonstra MC, Frangioni JV, van de Velde CJ, Vahrmeijer AL, Bonsing BA. Intraoperative near-infrared fluorescence imaging of a paraganglioma using methylene blue: A case report. Int J Surg Case Rep. 2015;6:150-3. doi: 10.1016/j.ijscr.2014.12.002. Epub 2014 Dec 05. PMID: 25541370; PMCID: PMC4334887.
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An adrenal mass and increased catecholamines: monoamine oxidase or pheochromocytoma effect?.

Journal of clinical medicine research

Bosscher MR, Wentholt IM, Ackermans MT, Nieveen van Dijkum EJ.
PMID: 25584109
J Clin Med Res. 2015 Mar;7(3):199-201. doi: 10.14740/jocmr2042w. Epub 2014 Dec 29.

Hormonal evaluation in patients with an adrenal incidentaloma can be difficult in patients with comorbidities or in patients using interfering drugs. We present a case of a 54-year-old man who was evaluated for an adrenal mass. The medical history...

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Bosscher MR, Wentholt IM, Ackermans MT, et al. An adrenal mass and increased catecholamines: monoamine oxidase or pheochromocytoma effect?. J Clin Med Res. 2014;7(3):199-201doi: 10.14740/jocmr2042w.
Bosscher, M. R., Wentholt, I. M., Ackermans, M. T., & Nieveen van Dijkum, E. J. (2015). An adrenal mass and increased catecholamines: monoamine oxidase or pheochromocytoma effect?. Journal of clinical medicine research, 7(3), 199-201. https://doi.org/10.14740/jocmr2042w
Bosscher, Marianne R F, et al. "An adrenal mass and increased catecholamines: monoamine oxidase or pheochromocytoma effect?." Journal of clinical medicine research vol. 7,3 (2015): 199-201. doi: https://doi.org/10.14740/jocmr2042w
Bosscher MR, Wentholt IM, Ackermans MT, Nieveen van Dijkum EJ. An adrenal mass and increased catecholamines: monoamine oxidase or pheochromocytoma effect?. J Clin Med Res. 2015 Mar;7(3):199-201. doi: 10.14740/jocmr2042w. Epub 2014 Dec 29. PMID: 25584109; PMCID: PMC4285070.
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Complete Remission in Metastatic Pheochromocytoma Treated with Extensive Surgery.

Cureus

Arnas-Leon C, Sánchez V, Santana Suárez AD, Quintana Arroyo S, Acosta C, Martinez Martin FJ.
PMID: 26918215
Cureus. 2016 Jan 05;8(1):e447. doi: 10.7759/cureus.447.

Pheochromocytomas are rare neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla. Malignant pheochromocytoma is defined as the presence of metastatic spread in tissues where chromaffin cells are not usually present. This case report describes the case...

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Arnas-Leon C, Sánchez V, Santana Suárez AD, et al. Complete Remission in Metastatic Pheochromocytoma Treated with Extensive Surgery. Cureus. 2016;8(1):e447doi: 10.7759/cureus.447.
Arnas-Leon, C., Sánchez, V., Santana Suárez, A. D., Quintana Arroyo, S., Acosta, C., & Martinez Martin, F. J. (2016). Complete Remission in Metastatic Pheochromocytoma Treated with Extensive Surgery. Cureus, 8(1), e447. https://doi.org/10.7759/cureus.447
Arnas-Leon, Claudia, et al. "Complete Remission in Metastatic Pheochromocytoma Treated with Extensive Surgery." Cureus vol. 8,1 (2016): e447. doi: https://doi.org/10.7759/cureus.447
Arnas-Leon C, Sánchez V, Santana Suárez AD, Quintana Arroyo S, Acosta C, Martinez Martin FJ. Complete Remission in Metastatic Pheochromocytoma Treated with Extensive Surgery. Cureus. 2016 Jan 05;8(1):e447. doi: 10.7759/cureus.447. PMID: 26918215; PMCID: PMC4744074.
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Mouse brain concentrations of 3-methoxytyramine and normetanephrine: a comparison of methods of sacrifice.

Neurochemistry international

Greene KA, Beck O, Faull KF, Stavinoha WB.
PMID: 20501202
Neurochem Int. 1988;12(1):47-52. doi: 10.1016/0197-0186(88)90147-7.

The identification of sacrifice methods that produce reliable measures of baseline central nervous system neurotransmitter concentrations poses a challenge to analytical neurochemical investigation. In the present study, microwave irradiation (MWVI) was compared with in situ freezing, cervical dislocation, and...

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Greene KA, Beck O, Faull KF, et al. Mouse brain concentrations of 3-methoxytyramine and normetanephrine: a comparison of methods of sacrifice. Neurochem Int. 1988;12(1):47-52doi: 10.1016/0197-0186(88)90147-7.
Greene, K. A., Beck, O., Faull, K. F., & Stavinoha, W. B. (1988). Mouse brain concentrations of 3-methoxytyramine and normetanephrine: a comparison of methods of sacrifice. Neurochemistry international, 12(1), 47-52. https://doi.org/10.1016/0197-0186(88)90147-7
Greene, K A, et al. "Mouse brain concentrations of 3-methoxytyramine and normetanephrine: a comparison of methods of sacrifice." Neurochemistry international vol. 12,1 (1988): 47-52. doi: https://doi.org/10.1016/0197-0186(88)90147-7
Greene KA, Beck O, Faull KF, Stavinoha WB. Mouse brain concentrations of 3-methoxytyramine and normetanephrine: a comparison of methods of sacrifice. Neurochem Int. 1988;12(1):47-52. doi: 10.1016/0197-0186(88)90147-7. PMID: 20501202.
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Aortoarteritis: Could it be a form of catecholamine-induced vasculitis?.

Indian journal of endocrinology and metabolism

Sarathi V, Lila AR, Bandgar TR, Shah NS.
PMID: 23776874
Indian J Endocrinol Metab. 2013 Jan;17(1):163-6. doi: 10.4103/2230-8210.107874.

Catecholamine-induced vasculitis is a well known but rarely described entity. However, aortoarteritis as a manifestation of catecholamine-induced vasculitis is not described in the literature. We have reported two patients in whom pheochromocytoma coexisted with aortoarteritis. Both patients were young...

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Sarathi V, Lila AR, Bandgar TR, et al. Aortoarteritis: Could it be a form of catecholamine-induced vasculitis?. Indian J Endocrinol Metab. 2013;17(1):163-6doi: 10.4103/2230-8210.107874.
Sarathi, V., Lila, A. R., Bandgar, T. R., & Shah, N. S. (2013). Aortoarteritis: Could it be a form of catecholamine-induced vasculitis?. Indian journal of endocrinology and metabolism, 17(1), 163-6. https://doi.org/10.4103/2230-8210.107874
Sarathi, Vijaya, et al. "Aortoarteritis: Could it be a form of catecholamine-induced vasculitis?." Indian journal of endocrinology and metabolism vol. 17,1 (2013): 163-6. doi: https://doi.org/10.4103/2230-8210.107874
Sarathi V, Lila AR, Bandgar TR, Shah NS. Aortoarteritis: Could it be a form of catecholamine-induced vasculitis?. Indian J Endocrinol Metab. 2013 Jan;17(1):163-6. doi: 10.4103/2230-8210.107874. PMID: 23776874; PMCID: PMC3659888.
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Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report.

Surgical case reports

Shibata M, Inaishi T, Miyajima N, Adachi Y, Takano Y, Nakanishi K, Takeuchi D, Noda S, Aita Y, Takekoshi K, Kodera Y, Kikumori T.
PMID: 29282558
Surg Case Rep. 2017 Dec 28;3(1):131. doi: 10.1186/s40792-017-0408-x.

BACKGROUND: Recent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). The clinical characteristics of hereditary PPGL are varying among the types of mutational genes. It is still difficult to specify the pathognomonic...

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Shibata M, Inaishi T, Miyajima N, et al. Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report. Surg Case Rep. 2017;3(1):131doi: 10.1186/s40792-017-0408-x.
Shibata, M., Inaishi, T., Miyajima, N., Adachi, Y., Takano, Y., Nakanishi, K., Takeuchi, D., Noda, S., Aita, Y., Takekoshi, K., Kodera, Y., & Kikumori, T. (2017). Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report. Surgical case reports, 3(1), 131. https://doi.org/10.1186/s40792-017-0408-x
Shibata, Masahiro, et al. "Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report." Surgical case reports vol. 3,1 (2017): 131. doi: https://doi.org/10.1186/s40792-017-0408-x
Shibata M, Inaishi T, Miyajima N, Adachi Y, Takano Y, Nakanishi K, Takeuchi D, Noda S, Aita Y, Takekoshi K, Kodera Y, Kikumori T. Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report. Surg Case Rep. 2017 Dec 28;3(1):131. doi: 10.1186/s40792-017-0408-x. PMID: 29282558; PMCID: PMC5745210.
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Pheochromocytoma of the Organ Zuckerkandl.

The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society

Lee C, Chang E, Gimenez J, McCarron R.
PMID: 28414676
J La State Med Soc. 2017 Mar-Apr;169(2):53. Epub 2017 Apr 15.

INTRODUCTION: Pheochromocytomas (PCCs);, or intra-adrenal paragangliomas (PGLs);, are neuroendocrine tumors arising within the adrenal medulla. Extra-adrenal paragangliomas may arise in the sympathetic or parasympathetic paraganglia and more rarely in other organs. One of the most common extra-adrenal sites is...

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Lee C, Chang E, Gimenez J, et al. Pheochromocytoma of the Organ Zuckerkandl. J La State Med Soc. 2017;169(2):53
Lee, C., Chang, E., Gimenez, J., & McCarron, R. (2017). Pheochromocytoma of the Organ Zuckerkandl. The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society, 169(2), 53.
Lee, C, et al. "Pheochromocytoma of the Organ Zuckerkandl." The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society vol. 169,2 (2017): 53.
Lee C, Chang E, Gimenez J, McCarron R. Pheochromocytoma of the Organ Zuckerkandl. J La State Med Soc. 2017 Mar-Apr;169(2):53. Epub 2017 Apr 15. PMID: 28414676.
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Myocardial Infarction with non-obstructed coronaries - atypical presentation of pheochromocytoma.

Endocrinology, diabetes & metabolism case reports

Melson E, Amir S, Shepherd L, Kauser S, Freestone B, Kempegowda P.
PMID: 31634865
Endocrinol Diabetes Metab Case Rep. 2019 Oct 19;2019. doi: 10.1530/EDM-19-0089. Epub 2019 Oct 19.

SUMMARY: Although pheochromocytoma classically presents with headaches, palpitations and paroxysmal hypertension, atypical presentations such as cardiomyopathy, stroke and subarachnoid haemorrhage have been infrequently documented. We present in this case report, an uncommon presentation of pheochromocytoma with myocardial infarction with...

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Melson E, Amir S, Shepherd L, et al. Myocardial Infarction with non-obstructed coronaries - atypical presentation of pheochromocytoma. Endocrinol Diabetes Metab Case Rep. 2019;2019doi: 10.1530/EDM-19-0089.
Melson, E., Amir, S., Shepherd, L., Kauser, S., Freestone, B., & Kempegowda, P. (2019). Myocardial Infarction with non-obstructed coronaries - atypical presentation of pheochromocytoma. Endocrinology, diabetes & metabolism case reports, 2019. https://doi.org/10.1530/EDM-19-0089
Melson, Eka, et al. "Myocardial Infarction with non-obstructed coronaries - atypical presentation of pheochromocytoma." Endocrinology, diabetes & metabolism case reports vol. 2019 (2019). doi: https://doi.org/10.1530/EDM-19-0089
Melson E, Amir S, Shepherd L, Kauser S, Freestone B, Kempegowda P. Myocardial Infarction with non-obstructed coronaries - atypical presentation of pheochromocytoma. Endocrinol Diabetes Metab Case Rep. 2019 Oct 19;2019. doi: 10.1530/EDM-19-0089. Epub 2019 Oct 19. PMID: 31634865.
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Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation.

Case reports in endocrinology

Rasquin L, Prater J, Mayrin J, Minimo C.
PMID: 30405919
Case Rep Endocrinol. 2018 Oct 14;2018:6358485. doi: 10.1155/2018/6358485. eCollection 2018.

BACKGROUND: Pheochromocytoma/paraganglioma is a rare tumor from neuroendocrine cells. 1/3CASE: 32-year-old male with incidental liver mass during laparoscopy for acute appendicitis. His symptoms included abdominal pain and profuse axillary hyperhidrosis. MRI showed an 11x12x14 cm cystic and solid mass...

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Rasquin L, Prater J, Mayrin J, et al. Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation. Case Rep Endocrinol. 2018;2018:6358485doi: 10.1155/2018/6358485.
Rasquin, L., Prater, J., Mayrin, J., & Minimo, C. (2018). Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation. Case reports in endocrinology, 20186358485. https://doi.org/10.1155/2018/6358485
Rasquin, Lorena, et al. "Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation." Case reports in endocrinology vol. 2018 (2018): 6358485. doi: https://doi.org/10.1155/2018/6358485
Rasquin L, Prater J, Mayrin J, Minimo C. Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation. Case Rep Endocrinol. 2018 Oct 14;2018:6358485. doi: 10.1155/2018/6358485. eCollection 2018. PMID: 30405919; PMCID: PMC6204204.
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A RETROPERITONEAL SEMINOMA WITH ENTRAPPED NERVE GANGLION MASQUERADING AS A PARAGANGLIOMA.

AACE clinical case reports

Rosenblum RC, Atlan K, Diment J, Mazeh H, Afek S, Rotman-Pikielny P, Twito O.
PMID: 31967062
AACE Clin Case Rep. 2019 Jun 26;5(5):e321-e325. doi: 10.4158/ACCR-2019-0251. eCollection 2019.

OBJECTIVE: The differential diagnosis of retroperito-neal tumors includes lymphoid, germ cell, and neurogenic tumors such as paraganglioma. Paragangliomas are rare neuroendocrine tumors of the autonomic nervous system, which may secrete catecholamines and their metabolites. Clinical features include sustained or...

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Rosenblum RC, Atlan K, Diment J, et al. A RETROPERITONEAL SEMINOMA WITH ENTRAPPED NERVE GANGLION MASQUERADING AS A PARAGANGLIOMA. AACE Clin Case Rep. 2019;5(5):e321-e325doi: 10.4158/ACCR-2019-0251.
Rosenblum, R. C., Atlan, K., Diment, J., Mazeh, H., Afek, S., Rotman-Pikielny, P., & Twito, O. (2019). A RETROPERITONEAL SEMINOMA WITH ENTRAPPED NERVE GANGLION MASQUERADING AS A PARAGANGLIOMA. AACE clinical case reports, 5(5), e321-e325. https://doi.org/10.4158/ACCR-2019-0251
Rosenblum, Rachel Chava, et al. "A RETROPERITONEAL SEMINOMA WITH ENTRAPPED NERVE GANGLION MASQUERADING AS A PARAGANGLIOMA." AACE clinical case reports vol. 5,5 (2019): e321-e325. doi: https://doi.org/10.4158/ACCR-2019-0251
Rosenblum RC, Atlan K, Diment J, Mazeh H, Afek S, Rotman-Pikielny P, Twito O. A RETROPERITONEAL SEMINOMA WITH ENTRAPPED NERVE GANGLION MASQUERADING AS A PARAGANGLIOMA. AACE Clin Case Rep. 2019 Jun 26;5(5):e321-e325. doi: 10.4158/ACCR-2019-0251. eCollection 2019. PMID: 31967062; PMCID: PMC6876950.
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Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging.

Endocrine connections

Rogowski-Lehmann N, Geroula A, Prejbisz A, Timmers HJLM, Megerle F, Robledo M, Fassnacht M, Fliedner S, Reincke M, Stell A, Januszewicz A, Lenders J, Eisenhofer G, Beuschlein F.
PMID: 30352425
Endocr Connect. 2018 Sep 01; doi: 10.1530/EC-18-0318. Epub 2018 Sep 01.

CONTEXT: Pheochromocytomas and paragangliomas (PPGLs) are rare but potentially harmful tumors that can vary in their clinical presentation. Tumors may be found due to signs and symptoms, as part of a hereditary syndrome or following an imaging procedure.OBJECTIVE: To...

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Rogowski-Lehmann N, Geroula A, Prejbisz A, et al. Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging. Endocr Connect. 2018;doi: 10.1530/EC-18-0318.
Rogowski-Lehmann, N., Geroula, A., Prejbisz, A., Timmers, H. J. L. M., Megerle, F., Robledo, M., Fassnacht, M., Fliedner, S., Reincke, M., Stell, A., Januszewicz, A., Lenders, J., Eisenhofer, G., & Beuschlein, F. (2018). Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging. Endocrine connections, . https://doi.org/10.1530/EC-18-0318
Rogowski-Lehmann, Natalie, et al. "Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging." Endocrine connections vol. (2018). doi: https://doi.org/10.1530/EC-18-0318
Rogowski-Lehmann N, Geroula A, Prejbisz A, Timmers HJLM, Megerle F, Robledo M, Fassnacht M, Fliedner S, Reincke M, Stell A, Januszewicz A, Lenders J, Eisenhofer G, Beuschlein F. Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging. Endocr Connect. 2018 Sep 01; doi: 10.1530/EC-18-0318. Epub 2018 Sep 01. PMID: 30352425; PMCID: PMC6215794.
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[Elevated level of methylated catecholamine derivatives is a pathognomic laboratory sign of pheochromocytoma].

Problemy endokrinologii

Kuznetsov NS, Beltsevich DG, Goncharov NP, Kats LY, Katsla GV, Kolesnikova GS, Ilyin AV, Melnichenko GA.
PMID: 31627629
Probl Endokrinol (Mosk). 2007 Feb 15;53(1):33-36. doi: 10.14341/probl200753133-36.

The levels of the methylated catecholamine derivatives (MCD) metanephrine and normetanephrine were measured in 46 patients operated on. The patients were divided into 2 groups: 1) 24 patients in whom chromaffinoma was histologically detected; their age varied from 9...

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Kuznetsov NS, Beltsevich DG, Goncharov NP, et al. [Elevated level of methylated catecholamine derivatives is a pathognomic laboratory sign of pheochromocytoma]. Probl Endokrinol (Mosk). 2007;53(1):33-36doi: 10.14341/probl200753133-36.
Kuznetsov, N. S., Beltsevich, D. G., Goncharov, N. P., Kats, L. Y., Katsla, G. V., Kolesnikova, G. S., Ilyin, A. V., & Melnichenko, G. A. (2007). [Elevated level of methylated catecholamine derivatives is a pathognomic laboratory sign of pheochromocytoma]. Problemy endokrinologii, 53(1), 33-36. https://doi.org/10.14341/probl200753133-36
Kuznetsov, N S, et al. "[Elevated level of methylated catecholamine derivatives is a pathognomic laboratory sign of pheochromocytoma]." Problemy endokrinologii vol. 53,1 (2007): 33-36. doi: https://doi.org/10.14341/probl200753133-36
Kuznetsov NS, Beltsevich DG, Goncharov NP, Kats LY, Katsla GV, Kolesnikova GS, Ilyin AV, Melnichenko GA. [Elevated level of methylated catecholamine derivatives is a pathognomic laboratory sign of pheochromocytoma]. Probl Endokrinol (Mosk). 2007 Feb 15;53(1):33-36. doi: 10.14341/probl200753133-36. Russian. PMID: 31627629.
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Showing 1 to 12 of 127 entries