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2,253 Possible Causes for Pheochromocytoma, Sensorineural Hearing Loss Associated with ELSTs

  • Von Hippel-Lindau Disease

    Finding Elusive Pheochromocytomas, by Graeme Eisenhofer Plasma Free Metanephrine and the Laboratory Evaluation for Pheochromocytoma, by David F.[web.archive.org] ) hearing loss, sensorineural, associated with elsts Genitourinary Kidneys: multiple renal cysts renal hemangioblastoma renal cell carcinoma (e.g., ) Genitourinary Internal[malacards.org] The majority of the patients had associated audiovestibular symptoms, including sensorineural hearing loss (84% of ears), tinnitus (73%), and vertigo (68%) that did not correlate[journal.frontiersin.org]

  • Panic Attacks

    Some or all of these symptoms can be found in the presence of a pheochromocytoma.[en.wikipedia.org] Some evidence suggests that hypoglycemia, hyperthyroidism, mitral valve prolapse, labyrinthitis, and pheochromocytoma may trigger or worsen panic disorder.[med.upenn.edu] ., palpitations, diaphoresis, tachycardia, heat intolerance) Hypoglycemia Pheochromocytoma (e.g., headache, diaphoresis, hypertension) Hypoparathyroidism (e.g., muscle cramps[emedicine.medscape.com]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Anxiety Disorder

    Bilateral disease was found in 12.5%, malignant pheochromocytoma in 29.6%, and hereditary forms in 23.0%.[doi.org] Mercado-Asis and Karel Pacak, Pheochromocytoma: Unmasking the Chameleon, Endocrine Hypertension, 10.1007/978-1-60761-548-4_7, (123-148), (2012).[doi.org] Some evidence suggests that hypoglycemia, hyperthyroidism, mitral valve prolapse, labyrinthitis, and pheochromocytoma may trigger or worsen panic disorder.[med.upenn.edu]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Hypertensive Crisis

    Pheochromocytoma is a catecholamine-producing tumor but rarely delayingly diagnosed until during pregnancy.[ncbi.nlm.nih.gov] Pheochromocytomas in pregnancy are rare but potentially lethal.[ncbi.nlm.nih.gov] Pheochromocytoma is a rare disease that may occur during pregnancy.[ncbi.nlm.nih.gov]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Labile Hypertension

    Perianesthetic risks and outcomes of pheochromocytoma and paraganglioma resection.[ndt.oxfordjournals.org] In addition, MRI scan of the adrenal glands may be helpful in further evaluation, as most adrenal pheochromocytomas are larger than 1 cm.[academic.oup.com] AU - Young, William Francis PY - 2004/4 Y1 - 2004/4 KW - Catecholamines KW - Hypertension KW - Paraganglioma KW - Pheochromocytoma UR - UR - U2 - 10.1093/ndt/gfg541 DO - 10.1093[mayoclinic.pure.elsevier.com]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Familial Pheochromocytoma

    During a 15-year period, 24 patients were treated operatively for pheochromocytoma at this medical center.[ncbi.nlm.nih.gov] Two patients had malignant pheochromocytoma. All except one patient with MEN had thyroid carcinoma. The two patients with malignant pheochromocytoma had MEN II.[ncbi.nlm.nih.gov] OBJECTIVE: To report the results of treatment of patients with familial pheochromocytomas in the laparoscopic era.[ncbi.nlm.nih.gov]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Hypertension

    Laparoscopic adrenalectomy was performed and confirmed a pheochromocytoma.[ncbi.nlm.nih.gov] Pheochromocytoma of the bladder is rare and accounts for less than 0.06% of all bladder neoplasms and less than 1% of all pheochromocytomas.[ncbi.nlm.nih.gov] Among them, primary aldosteronism, Cushing's Syndrome and pheochromocytoma are the most common cause of endocrine hypertension associated with an autonomous secretion of adrenal[ncbi.nlm.nih.gov]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Adrenal Cortical Adenoma

    METHODS: All patients with a pathological diagnosis of pheochromocytoma were evaluated for an ipsilateral cortical adenoma from 1994 through 2015.[ncbi.nlm.nih.gov] After right pheochromocytoma was diagnosed, right adrenalectomy was performed.[ncbi.nlm.nih.gov] Histologically, the right adrenal mass was compatible with pheochromocytoma, and the left adrenal mass was an adrenocortical adenoma.[ncbi.nlm.nih.gov]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Familial Medullary Thyroid Carcinoma

    Abstract Germline mutations of the three succinate dehydrogenase subunits SDHB, SDHC and SDHD have recently been associated with familial pheochromocytoma and paraganglioma[ncbi.nlm.nih.gov] Multiple endocrine neoplasia type 2A (MEN 2A) is characterized by MTC, pheochromocytomas, and parathyroid hyperplasia.[ncbi.nlm.nih.gov] […] multiple endocrine neoplasia type 2 (MEN2) syndromes and Hirschsprung's disease (HSCR) are inherited neurocristopathies characterized by medullary thyroid carcinoma (MTC), pheochromocytoma[ncbi.nlm.nih.gov]

    Missing: Sensorineural Hearing Loss Associated with ELSTs
  • Neurofibromatosis Type 1

    If not properly treated, pheochromocytoma has high maternal and fetal mortality rates.[ncbi.nlm.nih.gov] Pheochromocytoma and myocarditis should be considered when sudden death occurs in the setting of neurofibromatosis type 1.[ncbi.nlm.nih.gov] Our objective was to improve molecular diagnostics in patients with hereditary pheochromocytoma and paraganglioma (PPGL) by using next-generation sequencing (NGS) multi-gene[ncbi.nlm.nih.gov]

    Missing: Sensorineural Hearing Loss Associated with ELSTs

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