[Persistent low levels of human chorionic gonadotropin in the serum: investigation and management].

Harefuah

Department of Gynecology and Obstetrics, Ha'Emek Medical Center, Afula Rapapport Faculty of Medicine, Technion, Haifa.

Published: February 2009

Persistent low levels of human Chorionic Gonadotropin-hCG, the pregnancy hormone, in the serum in the absence of pregnancy or any evidence of Gestational Trophoblastic Disease (GTD) is a diagnostic and therapeutic dilemma. This condition mostly presents during follow-up after patients with a history of GTD or hydatidiform mole or an incidental pregnancy test. Many physicians are not aware of the broad differential diagnosis of this condition which is mostly benign. Therefore, many women with this condition have received chemotherapy and hysterectomy for assumed malignancy which were ineffective and unwarranted. The most common etiologies are: 1. Pituitary hCG: A condition mostly found in older women, completely benign and can be resolved using hormone replacement therapy or oral contraceptives. 2. False positive hCG: this condition has no clinical meaning, it can be identified by the absence of hCG in a parallel urine sample or using a better hCG test with no past reports of false positive. 3. Quiescent GTD: This is a benign trophoblastic disease in which the hyperglycosylated hCG accounts for a small percentage of the total hCG in the serum. Due to its premalignant nature, a follow-up of the hCG levels and the hyperglycosylated hCG percentage is needed. The hCG molecule has many forms. Different hCG tests detect different forms identified as heterogeneous in nature. For each etiology mentioned above there is a characteristic dominant form. If it was known which test to use, the diagnosis could be made.

Download full-text PDF

Source

Publication Analysis

Top Keywords

hcg
10
low levels
8
levels human
8
human chorionic
8
trophoblastic disease
8
hcg condition
8
false positive
8
hyperglycosylated hcg
8
condition
5
[persistent low
4

Similar Publications

Silver-Russell Syndrome (SRS) is a rare genetic disorder characterized by prenatal and postnatal growth restriction, distinctive facial features, and body asymmetry. Early suspicion during the first trimester remains challenging but crucial for optimizing clinical outcomes. This study aims to highlight a diagnostic approach to the early suspicion of SRS.

View Article and Find Full Text PDF

: Although preeclampsia (PE) and small for gestational age (SGA) are known to come from impaired placentation during the first trimester, prior studies have focused mostly on Doppler findings in the second trimester. : In this retrospective pilot study, we enrolled 628 singleton pregnant women who underwent ultrasound in both the first and second trimesters and blood test. For SGA correlation, we further excluded 12 subjects with PE because PE may be the cause of SGA.

View Article and Find Full Text PDF

Down syndrome with cryptorchidism and retroperitoneal mixed germ cell tumour in an adult patient: a case report and literature review.

World J Surg Oncol

January 2025

Department of Colorectal Surgery, Dingli Clinical College, Wenzhou Medical University (Wenzhou Central Hospital), 252 Baili East Road, Wenzhou, Zhejiang Province, 32500, China.

Background: An association between testicular cancer and Down syndrome has been reported by several studies. Down syndrome with cryptorchidism and retroperitoneal mixed germ cell tumours is rare, and yolk sac tumours are often considered secondary components of mixed germ cell tumours. Herein, we present a rare case of retroperitoneal mixed germ cell tumour with cryptorchidism accompanied by yolk sac tumour and seminoma in a patient with Down syndrome, along with its imaging features.

View Article and Find Full Text PDF

Objective: To compare pregnancy outcomes and serum progesterone levels between women who took sublingual (SL) progesterone lozenges versus intramuscular (IM) progesterone-in-oil for endometrial preparation and luteal support in programmed frozen embryo transfer (pFET) cycles.

Design: Retrospective cohort study.

Subjects: All patients who underwent pFET of a single euploid good-quality blastocyst between January 2018 and April 2023 at a single fertility center.

View Article and Find Full Text PDF

Triggering final follicular maturation for IVF cycles.

Reprod Biol Endocrinol

January 2025

Infertility and IVF Unit, Department of Obstetrics and Gynecology, Chaim Sheba Medical Center (Tel Hashomer), Ramat Gan, 52621, Israel.

As part of a conventional controlled ovarian hyperstimulation (COH) regimen, final follicular maturation is usually triggered by a single bolus dose of human chorionic gonadotropin (hCG). COH, which combines GnRH antagonist co-treatment with GnRH agonist(GnRHa) trigger, is often used in attempts to eliminate severe early ovarian hyperstimulation syndrome and to improve oocyte/embryo yield and quality. Recently, the combination of GnRHa, with hCG trigger has also been implemented into clinical practice.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!