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Pregnancy complicated with PFAPA (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis) syndrome: a case report

机译:妊娠并发PFPAA(周期性发热,口疮,口咽炎和宫颈腺炎)综合征:一例报告

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Periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA) syndrome has been considered as a childhood syndrome. The underlying etiology of PFAPA syndrome is unclear however, currently considered as auto-immune inflammatory disease. Recently, a few cases of adult-onset of PFAPA syndrome have been reported. However, there is no report about the successful management of pregnancy complicated with PFAPA syndrome. The patient was a 31-year-old woman who developed recurrent episodes of high fever associated with cervical adenitis, pharyngitis and vomiting started 9?months after a delivery. She was diagnosed with PFAPA syndrome and cimetidine 800?mg/day was initiated. Since then, these symptoms got better. Cimetidine treatment was discontinued since she became pregnant (6?weeks of pregnancy). Except one febrile episode at 8?weeks gestation, she did not develop a febrile episode during pregnancy. Peripheral blood Th1/Th2 ratio was decreased from the first trimester to the second trimester of pregnancy. Then again, the ratio was steadily elevated during the third trimester. At 38?weeks, she delivered a live born infant without any complication. Two months after delivery, she developed PFAPA syndrome again and cimetidine treatment was re-initiated. However, febrile episodes were not controlled well, and Th1/Th2 ratio was further elevated compared to pregnancy status. Colchicine 0.5?mg once a day was initiated. Symptoms were diminished and Th1/Th2 ratio was gradually decreased. There was no case report of pregnancy complicated with PFAPA syndrome, though there were several reports of adult-onset PFAPA cases without pregnancy. The current case may be the first case report of a successful pregnancy complicated with PFAPA. In this case, PFAPA symptoms were ameliorated during pregnancy, but reappeared after delivery. We speculate that PFAPA syndrome, a Th1 type immune disorder, might be improved due to the Th1 to Th2 shifting, which was induced by pregnancy. It is necessary to investigate further about PFAPA syndrome with pregnancy and Th1/Th2 immune responses in the future.
机译:周期性发热,口疮性口炎,咽炎和宫颈腺炎(PFAPA)综合征已被视为儿童期综合征。 PFAPA综合征的潜在病因尚不清楚,目前被认为是自身免疫性炎性疾病。近来,已经报道了几例成年的PFAPA综合征发病。但是,没有关于成功治疗妊娠合并PFAPA综合征的报道。该患者是一名31岁的妇女,在分娩后9个月开始出现反复发作的高热,并伴有宫颈腺炎,咽喉炎和呕吐。她被诊断出患有PFAPA综合征,并开始服用西咪替丁800 mg / day。从那时起,这些症状逐渐好转。西咪替丁自从怀孕(怀孕6周)以来就停止治疗。除了在妊娠8周时出现一次高热发作外,她在怀孕期间未出现高热发作。从妊娠的前三个月到怀孕的三个月,外周血Th1 / Th2比率降低。然后,该比率在孕晚期稳定增加。在38周时,她分娩了一个没有任何并发​​症的活产婴儿。分娩后两个月,她再次出现PFAPA综合征,西咪替丁治疗重新开始。然而,与妊娠状态相比,高热发作没有得到很好的控制,Th1 / Th2比值进一步升高。每天一次开始使用秋水仙碱0.5?mg。症状减轻,Th1 / Th2比率逐渐降低。尽管有几例成人妊娠而无妊娠的PFAPA病例报告,但没有妊娠并发PFAPA综合征的病例报告。当前病例可能是成功妊娠合并PFAPA的首例病例。在这种情况下,PFAPA症状在怀孕期间得到缓解,但在分娩后再次出现。我们推测,由于怀孕引起的Th1向Th2转移,可能会改善Th1型免疫疾病PFAPA综合征。将来有必要进一步研究妊娠期PFAPA综合征和Th1 / Th2免疫反应。

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