Computed tomography-guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patients. Griffing, E., Reading, B., De Luca, F., Agne, D., Juang, D., & Halpin, K. Journal of pediatric endocrinology & metabolism: JPEM, 37(7):657–662, July, 2024. doi abstract bibtex OBJECTIVES: Pheochromocytomas (PHEO) are neuroendocrine tumors rarely diagnosed in children. We are reporting on the management challenges of three adolescent patients who present with hereditary PHEO. CASE PRESENTATION: The index patient and his male sibling presented with bilateral PHEO, while a third patient presented with a unilateral PHEO, all associated with von Hippel-Lindau (VHL) syndrome. The patients were treated with computed tomography (CT)-guided percutaneous cryoablation (CRA) of the adrenal lesions, with varying degrees of success. CONCLUSIONS: CT-guided percutaneous CRA of hereditary PHEO has not been reported in the pediatric population and may represent a novel treatment strategy that reduces the risk of intraprocedural complications and adrenal insufficiency (AI).
@article{griffing_computed_2024,
title = {Computed tomography-guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patients},
volume = {37},
issn = {2191-0251},
doi = {10.1515/jpem-2024-0033},
abstract = {OBJECTIVES: Pheochromocytomas (PHEO) are neuroendocrine tumors rarely diagnosed in children. We are reporting on the management challenges of three adolescent patients who present with hereditary PHEO.
CASE PRESENTATION: The index patient and his male sibling presented with bilateral PHEO, while a third patient presented with a unilateral PHEO, all associated with von Hippel-Lindau (VHL) syndrome. The patients were treated with computed tomography (CT)-guided percutaneous cryoablation (CRA) of the adrenal lesions, with varying degrees of success.
CONCLUSIONS: CT-guided percutaneous CRA of hereditary PHEO has not been reported in the pediatric population and may represent a novel treatment strategy that reduces the risk of intraprocedural complications and adrenal insufficiency (AI).},
language = {eng},
number = {7},
journal = {Journal of pediatric endocrinology \& metabolism: JPEM},
author = {Griffing, Emily and Reading, Brenton and De Luca, Francesco and Agne, Daniel and Juang, David and Halpin, Kelsee},
month = jul,
year = {2024},
pmid = {38807486},
keywords = {Adolescent, Adrenal Gland Neoplasms, Child, Cryosurgery, Female, Humans, Male, Pheochromocytoma, Prognosis, Tomography, X-Ray Computed, adrenal insufficiency, pheochromocytoma, von Hippel-Lindau Disease, von Hippel–Lindau syndrome},
pages = {657--662},
}
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The patients were treated with computed tomography (CT)-guided percutaneous cryoablation (CRA) of the adrenal lesions, with varying degrees of success. 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We are reporting on the management challenges of three adolescent patients who present with hereditary PHEO.\nCASE PRESENTATION: The index patient and his male sibling presented with bilateral PHEO, while a third patient presented with a unilateral PHEO, all associated with von Hippel-Lindau (VHL) syndrome. 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