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D35.00 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM D35.00 became effective on October 1, 2024. This is the American ICD-10-CM version of D35.00 - other international versions of ICD-10 D35.00 may differ.
- D35.1
D35.1 is a billable/specific ICD-10-CM code that can be used...
- Pheochromocytoma
ICD-10-CM Diagnosis Code C74.10 Malignant neoplasm of...
- D35.1
ICD-10-CM Diagnosis Code C74.10 Malignant neoplasm of medulla of unspecified adrenal gland 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 Billable/Specific Code
8 Μαΐ 2023 · Abstract. Objective. The aim of this review was to provide a practical approach for clinicians regarding the diagnosis and management of pheochromocytomas and paragangliomas (PPGLs). Methods. A literature search of PubMed was carried out using key words, including pheochromocytoma, paraganglioma, treatment, diagnosis, screening, and management.
26 Δεκ 2021 · Introduction. Nonmalignant tumor of adrenal medulla. most common adrenal tumor in adults. vs neuroblastoma, which is most common in children. secretes catecholamines causing episodic hypertension. Rule of 10’s. 10% malignant. 10% bilateral. 10% extra-adrenal. bladder and organ of Zuckerkandl (bifurcation of aorta) 10% calcify. 10% kids.
28 Μαρ 2019 · Pancreatic neuroendocrine tumors (also called islet cell tumors) – This type of tumor typically arises in the pancreas, although they can also occur outside the pancreas. Pheochromocytoma – This is a rare type of NET that typically develops in the adrenal gland, but can also arise in other parts of the body.
28 Αυγ 2024 · Clinical presentation. It is a rare but classical cause of uncontrolled secondary hypertension, with a minority having superimposed paroxysmal hypertensive crises 11. Patients may also present with cardiac dysfunction (myocardial infarction, pulmonary edema) or neurological events (severe headache, visual disturbance, hemorrhagic strokes) 5.
7 Φεβ 2017 · Catecholamine secreting tumor that may cause life-threatening hypertension episodes/cardiac arrhythmias. Pheochromocytoma: tumor arising from adrenomedullary chromaffin cells that: Commonly produces one or more catecholamines: epinephrine, norepinephrine, and dopamine. Are rarely biochemically silent
