A case of pregnancy with a uterine fibroid produced parathyroid hormone related protein

A 30-year-old primigravid, nulliparous woman was diagnosed with uterine fibroid 6 cm in diameter, and had been followed up. She became pregnant by embryo transplantation and was referred to our hospital at the 7th week of gestation. She was admitted at 13 weeks and 3 days of pregnancy due to hypereme...

Full description

Saved in:
Bibliographic Details
Published inJournal of Japan Society of Perinatal and Neonatal Medicine Vol. 60; no. 2; pp. 250 - 255
Main Authors Arahori, Kenji, Tannaka, Shiori, Hayashi, Kana, Takatsuji, Noriko, Kato, Yuichiro
Format Journal Article
LanguageJapanese
Published Japan Society of Perinatal and Neonatal Medicine 2024
一般社団法人 日本周産期・新生児医学会
Subjects
Online AccessGet full text
ISSN1348-964X
2435-4996
DOI10.34456/jjspnm.60.2_250

Cover

More Information
Summary:A 30-year-old primigravid, nulliparous woman was diagnosed with uterine fibroid 6 cm in diameter, and had been followed up. She became pregnant by embryo transplantation and was referred to our hospital at the 7th week of gestation. She was admitted at 13 weeks and 3 days of pregnancy due to hyperemesis, and an abnormally high blood Ca level of 16.0 mg/dL. Because of a low intact-parathyroid hormone(PTH)and high parathyroid hormone-related peptide(PTHrP)and 1, 25-dihydroxyvitamin D levels, a PTHrP-producing tumor was suspected. We did not find malignant PTHrP-producing tumor. Although the blood Ca level decreased by fluid replacement, it increased again with mild impairment of renal function. As the uterine fibroid was suspected to be a PTHrP-producing tumor, abdominal myomectomy was performed at 15 weeks and 5 days of pregnancy. Both the Ca and PTHrP levels decreased on day 1 after surgery with relief of symptoms, and she was discharged. Histopathological examination indicated uterine leiomyoma accompanied by liquefaction degeneration, and the uterine fibroid was diagnosed by immunostaining as a PTHrP-producing tumor. Since uterine fibroid producing PTHrP tumor is rare, the case is reported with a review of the literature.
ISSN:1348-964X
2435-4996
DOI:10.34456/jjspnm.60.2_250