Introduction: Identification of pheochromocytoma during pregnancy is unusual. Lack of appropriate management may be responsible of high risk for both mother and fetus. The guarantee of a successful management of a pheochromocytoma during pregnancy is the establishment of an early diagnosis as well as the prevention of a hypertensive crisis during delivery and surgical treatment and without compromising the maternal-fetal prognosis.
Case Presentation: A 31-year-old female patient, without any notable pathological history, pregnant at 20 weeks of amenorrhea was diagnosed for a Menard's triad. The medical investigations had allowed to confirm the diagnosis of left secretory pheochromocytoma. The surgical indication was taken in concertation between surgeons, endocrinologists, gynecologists and anesthesiologists. The parturient had undergone an uneventful laparoscopic left adrenalectomy without incidents.
Case Discussion: Our case well illustrates that when the operative indication is posed, laparoscopic surgery can be performed safely during any trimester. However, it is legitimate to modulate the incisions according to gestational age and the height of the fundus. The involvement of all disciplines intervening in the management of the pregnant woman with pheochromocytoma is the guarantor of a favorable maternal-fetal prognosis.
Conclusion: A well-established diagnosis for pregnant women with severe secondary hypertension, multidisciplinary management, and safe laparoscopic approach are crucial to prevent perinatal morbidity and mortality.
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http://dx.doi.org/10.1016/j.ijscr.2023.108483 | DOI Listing |
Cureus
October 2024
Anesthesiology, Unidade Local de Saúde do Alto Ave, Guimarães, PRT.
Gynecol Obstet Fertil Senol
October 2024
Gynécologie-obstétrique et médecine de la reproduction, CHU de Caen, avenue de la Côte de Nacre, 14000 Caen, France; UFR médecine Caen, rue des Rochambelles, 14000 Caen, France.
Objectives: Carrying out a pregnancy to term in a patient with a paraganglioma or pheochromocytoma (PPGL) results from a multidisciplinary challenge. The objective was to compare our therapeutic attitude with the existing literature and to identify optimal treatment.
Methods: Description of a case of paraganglioma treated during pregnancy at the University Hospital Center of Caen (France) in 2024 and comparison with the literature.
Best Pract Res Clin Endocrinol Metab
December 2024
Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Cureus
May 2024
Obstetrics and Gynecology, Unidade Local de Saúde (ULS) de Braga, Braga, PRT.
Pheochromocytoma, a rare but potentially serious condition, poses challenges in timely identification, especially during pregnancy due to misconceptions about pregnancy-related hypertension causes. However, paroxysmal symptoms heighten diagnostic suspicion. The diagnosis relies on biochemical confirmation of catecholamine hypersecretion followed by imaging for tumor localization.
View Article and Find Full Text PDFJCEM Case Rep
July 2024
McMaster University, Division of Endocrinology and Metabolism, Hamilton, ON L8S 4L8, Canada.
The diagnosis of pheochromocytoma or paraganglioma (PGL) during pregnancy is extremely rare, with 2 large case series suggesting that the prevalence is between 0.0002% and 0.007%.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!