Pheochromocytoma presenting as partial HELLP syndrome
Diagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the pat...
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2015
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| Online Access: | http://hdl.handle.net/10725/10695 http://dx.doi.org/10.1155/2015/294326 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://www.hindawi.com/journals/criog/2015/294326/abs/ |
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| _version_ | 1864513487102803968 |
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| author | Daaboul, Yazan |
| author2 | Korjian, Serge Khalil, Lamis Nemr, Rita |
| author2_role | author author author |
| author_facet | Daaboul, Yazan Korjian, Serge Khalil, Lamis Nemr, Rita |
| author_role | author |
| dc.creator.none.fl_str_mv | Daaboul, Yazan Korjian, Serge Khalil, Lamis Nemr, Rita |
| dc.date.none.fl_str_mv | 2015 2019-05-29T11:25:52Z 2019-05-29T11:25:52Z 2019-05-29 |
| dc.identifier.none.fl_str_mv | 2090-6692 http://hdl.handle.net/10725/10695 http://dx.doi.org/10.1155/2015/294326 Daaboul, Y., Korjian, S., Khalil, L., & Nemr, R. (2015). Pheochromocytoma presenting as partial HELLP syndrome. Case reports in obstetrics and gynecology, 2015. http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://www.hindawi.com/journals/criog/2015/294326/abs/ |
| dc.language.none.fl_str_mv | en |
| dc.relation.none.fl_str_mv | Case Reports in Obstetrics and Gynecology |
| dc.rights.*.fl_str_mv | info:eu-repo/semantics/openAccess |
| dc.title.none.fl_str_mv | Pheochromocytoma presenting as partial HELLP syndrome |
| dc.type.none.fl_str_mv | Article info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article |
| description | Diagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the patient underwent urgent cesarean section. The patient gave birth to a viable baby, but she sustained an episode of ventricular fibrillation intraoperatively that did not result in any long-term sequelae. The patient’s symptoms persisted postoperatively and work-up for secondary etiologies of hypertension demonstrated a right adrenal pheochromocytoma. Following resection, the patient’s signs and symptoms resolved, and her lab tests normalized. |
| eu_rights_str_mv | openAccess |
| format | article |
| id | LAURepo_09faca6fbb13e20af292331d989a8d40 |
| identifier_str_mv | 2090-6692 Daaboul, Y., Korjian, S., Khalil, L., & Nemr, R. (2015). Pheochromocytoma presenting as partial HELLP syndrome. Case reports in obstetrics and gynecology, 2015. |
| language_invalid_str_mv | en |
| network_acronym_str | LAURepo |
| network_name_str | Lebanese American University repository |
| oai_identifier_str | oai:laur.lau.edu.lb:10725/10695 |
| publishDate | 2015 |
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| spelling | Pheochromocytoma presenting as partial HELLP syndromeDaaboul, YazanKorjian, SergeKhalil, LamisNemr, RitaDiagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the patient underwent urgent cesarean section. The patient gave birth to a viable baby, but she sustained an episode of ventricular fibrillation intraoperatively that did not result in any long-term sequelae. The patient’s symptoms persisted postoperatively and work-up for secondary etiologies of hypertension demonstrated a right adrenal pheochromocytoma. Following resection, the patient’s signs and symptoms resolved, and her lab tests normalized.PublishedN/A2019-05-29T11:25:52Z2019-05-29T11:25:52Z20152019-05-29Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2090-6692http://hdl.handle.net/10725/10695http://dx.doi.org/10.1155/2015/294326Daaboul, Y., Korjian, S., Khalil, L., & Nemr, R. (2015). Pheochromocytoma presenting as partial HELLP syndrome. Case reports in obstetrics and gynecology, 2015.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://www.hindawi.com/journals/criog/2015/294326/abs/enCase Reports in Obstetrics and Gynecologyinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/106952021-03-19T10:45:19Z |
| spellingShingle | Pheochromocytoma presenting as partial HELLP syndrome Daaboul, Yazan |
| status_str | publishedVersion |
| title | Pheochromocytoma presenting as partial HELLP syndrome |
| title_full | Pheochromocytoma presenting as partial HELLP syndrome |
| title_fullStr | Pheochromocytoma presenting as partial HELLP syndrome |
| title_full_unstemmed | Pheochromocytoma presenting as partial HELLP syndrome |
| title_short | Pheochromocytoma presenting as partial HELLP syndrome |
| title_sort | Pheochromocytoma presenting as partial HELLP syndrome |
| url | http://hdl.handle.net/10725/10695 http://dx.doi.org/10.1155/2015/294326 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://www.hindawi.com/journals/criog/2015/294326/abs/ |