Levy Chanan, Pereira Leonardo, Dardarian Thomas, Cardonick Elyce
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Thomas Jefferson University, Pennsylvania Hospital, Philadelphia, USA.
J Reprod Med. 2004 Jan;49(1):61-4.
Solid pseudopapillary tumor (SPT) of the pancreas is a rare neoplasm, occurring predominantly in young African American women. Tumor growth, which is typically slow, may be accelerated during pregnancy secondary to the influence of progesterone.
We report a rare case of an 8-cm SPT in the head of the pancreas presenting as hyperemesis gravidarum during pregnancy. In contrast to previous case reports, surgical resection of the tumor at 16 weeks' gestation, although successful, did not ameliorate the patient's abdominal pain, nausea or vomiting. With intravenous nutritional support, she delivered a healthy infant near term.
SPT may present as hyperemesis gravidarum. Patients with refractory hyperemesis gravidarum should be evaluated for thyroid disease, gastroesophageal reflux, cholestasis and pancreatitis. If these more common etiologies are excluded, then one may consider SPT in the differential diagnosis, particularly in African American patients. SPT may grow during pregnancy due to progesterone responsiveness. Surgical resection during pregnancy is possible without harmful fetal effects but may not correct gastrointestinal dysfunction during pregnancy.
胰腺实性假乳头状瘤(SPT)是一种罕见的肿瘤,主要发生在年轻的非裔美国女性中。肿瘤生长通常缓慢,在孕期受孕酮影响可能加速。
我们报告一例罕见的胰腺头部8厘米SPT病例,该病例在孕期表现为妊娠剧吐。与既往病例报告不同,妊娠16周时对肿瘤进行手术切除,尽管手术成功,但并未改善患者的腹痛、恶心或呕吐症状。通过静脉营养支持,她在接近足月时产下一名健康婴儿。
SPT可能表现为妊娠剧吐。难治性妊娠剧吐患者应评估是否患有甲状腺疾病、胃食管反流、胆汁淤积和胰腺炎。如果排除了这些更常见的病因,那么在鉴别诊断时可考虑SPT,尤其是在非裔美国患者中。由于对孕酮有反应,SPT在孕期可能生长。孕期进行手术切除对胎儿无不良影响,但可能无法纠正孕期的胃肠功能障碍。