INTRAMURAL ISTHMIC PREGNANCY FOLLOWING PREVIOUS CESAREAN SECTION AND IN VITRO FERTILIZATION: A CASE REPORT WITH DISCUSSION OF THE MOLECULAR PATHOLOGY OF CESAREAN SCAR IMPLANTATION

In: Genetics and Molecular Research · 2026 · doi:10.4238/hsj64627 · W7197028534
Case report OA: hybrid CC0
⚙ AI-generated summary by qwen3.7-flash, 2026-10-04 ⓘ

This case report describes a fertility-preserving treatment for intramural isthmic pregnancy following cesarean section and IVF, while discussing the molecular pathology of cesarean scar implantation involving extracellular matrix remodeling and endometrial receptivity markers.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

⚙ AI-generated deep summary by qwen3.7-flash, 2026-09-29 · read from full text ⓘ

This case report describes a 35-year-old woman with secondary infertility who developed an intramural isthmic pregnancy at seven weeks gestation following frozen embryo transfer. High-resolution imaging confirmed complete myometrial encasement of the gestational sac, leading to treatment via laparoscopic excision and local methotrexate injection to preserve fertility. The authors discuss the molecular pathology of cesarean scar implantation, highlighting altered expression of matrix metalloproteinases, integrin β3, and leukemia inhibitory factor in endometrial receptivity. Relevance to endometriosis: listed as one indication for GnRH antagonists, though the paper's main focus is uterine fibroids.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Intramural pregnancy is among the rarest forms of ectopic implantation, accounting for fewer than 1% of ectopic pregnancies, and is associated with a high risk of uterine rupture and life-threatening hemorrhage when the diagnosis is delayed. The molecular pathology of abnormal implantation at the cesarean scar and lower uterine segment is increasingly being defined and involves altered expression of extracellular matrix remodeling enzymes, dysregulated wound-healing pathways, and changes in endometrial receptivity markers. We report a 35-year-old woman with a previous cesarean section and secondary infertility who conceived following frozen embryo transfer and was diagnosed with an intramural isthmic pregnancy at 7 weeks of gestation. The diagnosis was established by high-resolution transvaginal ultrasonography and confirmed by pelvic magnetic resonance imaging, both of which demonstrated complete myometrial encasement of the gestational sac without communication with the endometrial cavity. A fertility-preserving combined approach was used, comprising laparoscopic excision of the gestational tissue with site-directed local methotrexate injection into the surrounding myometrial bed. The myometrial defect was repaired in two layers and the uterus was preserved. Serial beta-human chorionic gonadotropin titers fell from 38,640 mIU/mL preoperatively to 112 mIU/mL by postoperative day 21. Histopathology confirmed chorionic villi embedded entirely within myometrial smooth muscle fibers, without intervening decidualized endometrium. The case is discussed in the context of recent molecular and gene-expression studies of cesarean scar healing and lower-segment implantation, including data on the connective tissue growth factor (CTGF)–LRP1 axis, matrix metalloproteinase expression, integrin β3 and leukemia inhibitory factor as endometrial receptivity markers, and microRNA dysregulation at the cesarean scar niche.
Full text 2,489 characters · extracted from oa-doi-fallback · click to expand
INTRAMURAL ISTHMIC PREGNANCY FOLLOWING PREVIOUS CESAREAN SECTION AND IN VITRO FERTILIZATION: A CASE REPORT WITH DISCUSSION OF THE MOLECULAR PATHOLOGY OF CESAREAN SCAR IMPLANTATION DOI: https://doi.org/10.4238/hsj64627Keywords: Intramural pregnancy; cesarean scar; gene expression; matrix metalloproteinase; integrin β3; leukemia inhibitory factor; microRNA; in vitro fertilization; fertility preservation.Abstract Intramural pregnancy is among the rarest forms of ectopic implantation, accounting for fewer than 1% of ectopic pregnancies, and is associated with a high risk of uterine rupture and life-threatening hemorrhage when the diagnosis is delayed. The molecular pathology of abnormal implantation at the cesarean scar and lower uterine segment is increasingly being defined and involves altered expression of extracellular matrix remodeling enzymes, dysregulated wound-healing pathways, and changes in endometrial receptivity markers. We report a 35-year-old woman with a previous cesarean section and secondary infertility who conceived following frozen embryo transfer and was diagnosed with an intramural isthmic pregnancy at 7 weeks of gestation. The diagnosis was established by high-resolution transvaginal ultrasonography and confirmed by pelvic magnetic resonance imaging, both of which demonstrated complete myometrial encasement of the gestational sac without communication with the endometrial cavity. A fertility-preserving combined approach was used, comprising laparoscopic excision of the gestational tissue with site-directed local methotrexate injection into the surrounding myometrial bed. The myometrial defect was repaired in two layers and the uterus was preserved. Serial beta-human chorionic gonadotropin titers fell from 38,640 mIU/mL preoperatively to 112 mIU/mL by postoperative day 21. Histopathology confirmed chorionic villi embedded entirely within myometrial smooth muscle fibers, without intervening decidualized endometrium. The case is discussed in the context of recent molecular and gene-expression studies of cesarean scar healing and lower-segment implantation, including data on the connective tissue growth factor (CTGF)–LRP1 axis, matrix metalloproteinase expression, integrin β3 and leukemia inhibitory factor as endometrial receptivity markers, and microRNA dysregulation at the cesarean scar niche. Downloads Published Issue Section License This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

⚙ Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback ⓘ

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2026) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

openalex
last seen: 2026-08-14T06:05:18.289012+00:00
License: CC0 · commercial use OK