Rejected at 10:56 p.m. Feb, 17, 2024 ] by herstein.jacob
Author: mtstralser
Related Note: 1516031999666
Rationale for change

AMBOSS and StatPearls (https://www.ncbi.nlm.nih.gov/books/NBK549834/) say paragangliomas arise from chromaffin cells. Also, if I am understanding uptodate correctly, the understanding is that they are not glomus cells. "All were previously referred to as chemodectomas. However, this is a misnomer, since only the carotid body paraganglia act as chemoreceptors [7]; this term should no longer be used. Older terms for tumors of the jugular paraganglia (glomus jugulare) and the tympanic paraganglia (glomus tympanicum) should also no longer be used; the term jugulotympanic paraganglioma is preferred [8]. (See 'Hereditary syndromes' below.)"

Rejection reason

Paragangliomas originate from paraganglia in chromaffin-negative glomus cells

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#AK_Step1_v12::#FirstAid::08_Endocrine::04_Pathology::24_Pheochromocytoma::02_Symptoms::*Paraganglioma #AK_Step1_v12::^Systems::Endocrine::BGadds #AK_Other::#AK_Original_Decks::Step_1::Zanki_Step_Decks::Zanki_Endocrine::Endocrine_Pathology #AK_Other::^EXPN::BGadd #AK_Step1_v12::#OME::04_Organ_Systems::06_Endocrine::02_Adrenal::04_Adrenal_Hyperplasia_NOS #AK_Step1_v12::#FirstAid::08_Endocrine::04_Pathology::24_Pheochromocytoma #AK_Step1_v12::#OME::PreClinical::04_Organ_Systems::06_Endocrine::02_Adrenal::04_Adrenal_Hyperplasia_NOS #AK_Other::Only_Step_1 #AK_Step1_v12::#FirstAid::11_Musculoskeletal_Skin_and_Connective_Tissue::03_Derm::09_Vascular_tumors_of_skin::04_Glomus_tumor #AK_Step1_v12::#SketchyPath::07_Endocrine::02_Adrenal_Disorders::05_Pheochromocytoma_&_Neuroblastoma #AK_Step1_v12::#Low/HighYield::5-LowYield