Auswahl der wissenschaftlichen Literatur zum Thema „Ovarian paraganglioma“

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Zeitschriftenartikel zum Thema "Ovarian paraganglioma"

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ETTAOUSSI, Abdelhak, Khalid JAMALEDDINE, Abdessamad MAJD, et al. "Incidental Ovarian Paraganglioma in a 62-Year-Old Woman: A Case Report of Diagnostic Challenge and Surgical Management." INTERNATIONAL JOURNAL OF HEALTH & MEDICAL RESEARCH 04, no. 03 (2025): 143–47. https://doi.org/10.5281/zenodo.15030718.

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Paragangliomas are rare neuroendocrine tumors originating from chromaffin cells of the neural crest. While they typically occur in the adrenal medulla as pheochromocytomas or along the sympathetic and parasympathetic chains, paragangliomas in the female genital tract are exceptionally uncommon. This report presents a case of a large right ovarian paraganglioma in a 62-year-old woman with a medical history of hypertension and diabetes. She presented with abdominal pain and fever, which led to a diagnosis of appendicitis, though an unexpected adnexal mass was discovered during surgery. Histologi
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Pedroso, Célia, Raquel Robalo, Pedro Sereno, Carlos Barros, and Carlos Marques. "A Rare Abdomino-Pelvic Tumor: Paraganglioma." Acta Médica Portuguesa 28, no. 1 (2015): 114. http://dx.doi.org/10.20344/amp.5403.

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<p>Paragangliomas are rare tumors, with a reported incidence of 2–8 per million. They are chromaffin cell tumors that develop from the neural crest cells and may be divided in tumors derived from the parasympathetic or sympathetic ganglia. We report a case a of a 32-year-old nulliparous woman, referred to our Infertility Clinic. Abdomino-pelvic ultrasound identified a large abdominopelvic tumor, without ovarian origin (both ovaries were identified and had normal morphology). Magnetic Resonance Imaging suggested a right adnexal multicystic, vascularized mass close to iliac vessels and que
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Schuldt, Maolly, Juan Antonio Retamero, Malvina Tourné, and Francisco F. Nogales. "Ovarian Paraganglioma." International Journal of Surgical Pathology 23, no. 2 (2014): 130–33. http://dx.doi.org/10.1177/1066896914526779.

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Kumar, Manish, Aashima Dabas, Vivek Manchanda, Nidhi Mahajan, and Kaustuv Mitra. "Hyponatremic-Hypertensive Syndrome in Ovarian Paraganglioma." Indian Pediatrics 56, no. 1 (2019): 69–71. http://dx.doi.org/10.1007/s13312-019-1472-z.

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Elliot, Victoria J., Emily C. Shaw, Mark Walker, Eleanor Jaynes, and Jeffery M. Theaker. "Ovarian Paraganglioma Arising From Mature Cystic Teratoma." International Journal of Gynecological Pathology 31, no. 6 (2012): 545–46. http://dx.doi.org/10.1097/pgp.0b013e31824d3564.

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Alli, Kasumawati, Basri Johan Jeet Abdullah, Collin Ng Leong Liong, and Eugene Leong Weng Kong. "Left retroperitoneal paraganglioma with enlarged ovarian vessels." European Journal of Radiology Extra 67, no. 1 (2008): 29–32. http://dx.doi.org/10.1016/j.ejrex.2008.04.011.

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Lim, Eng Seng, Hwee Ching Tee, and Jin Hui Ho. "UNVEILING THE UNEXPECTED." Journal of the ASEAN Federation of Endocrine Societies 40, S1 (2025): 97–98. https://doi.org/10.15605/jafes.040.s1.166.

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INTRODUCTION/BACKGROUNDParagangliomas are rare neuroendocrine tumors that arise from extra-adrenal paraganglionic tissue, typically associated with the autonomic nervous system. While they are most commonly found in the adrenal medulla (as pheochromocytomas) or along the sympathetic and parasympathetic chains, their occurrence in the paraovarian region is extremely rare. CASEWe present the case of a 42-year-old female with a history of left external iliac and common femoral vein thrombosis, who presented with progressive abdominal distension over the past six months. She was normotensive and e
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Chishima, Fumihisa, Masaaki Tamura, Teine Nakazawa, et al. "Paraaortic paraganglioma arising in an ovarian carcinoma patient mimicking lymph node metastasis." Journal of Obstetrics and Gynaecology Research 36, no. 1 (2010): 204–8. http://dx.doi.org/10.1111/j.1447-0756.2009.01094.x.

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Sahin, Gozde, Ceyhan Ugurluoglu, Serra Akar, Ayhan Gul, Aysegul Kebapcilar, and Cetin Celik. "Para-aortic paraganglioma mimicking lymph node metastasis in an ovarian carcinoma: a case report." Journal of Obstetrics and Gynaecology 38, no. 6 (2018): 882–84. http://dx.doi.org/10.1080/01443615.2017.1404013.

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Bizzarri, Nicolò, Franco De Cian, Stefano Di Domenico, et al. "Peritoneal carcinomatosis from ovarian paraganglioma: Report of a rare case and systematic review of the literature." Journal of Obstetrics and Gynaecology Research 44, no. 9 (2018): 1682–92. http://dx.doi.org/10.1111/jog.13713.

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Bücher zum Thema "Ovarian paraganglioma"

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Jolly, Elaine, Andrew Fry, and Afzal Chaudhry, eds. Endocrine. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199230457.003.0007.

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Chapter 7 covers the basic science and clinical topics relating to the endocrine system which trainees are required to learn as part of their basic training and demonstrate in the MRCP. It covers endocrine physiology, acid-base balance, thyrotoxicosis, hypothyroidism, goitre and thyroid nodule, Cushing syndrome, acromegaly, hyperprolactinaemia, hypopituitarism, diabetes insipidus, adrenal incidentaloma, primary hyperaldosteronism, adrenal insufficiency, phaeochromocytoma and paraganglioma , male hypogonadism and Gynaecomastia, menstrual disorders and anovulation, hirsutism and the polycystic o
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