Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25746
Title: Ruptured salpingitis isthmica nodosa: a rare cause for spontaneous haemoperitoneum.
Austin Authors: Huang, Dora ;Lowe, Sandon;Kumaran, Pravena;Choy, Kay T 
Affiliation: Surgery
Department of Surgery, North West Regional Hospital, Burnie, Tasmania, Australia
Issue Date: 26-Jan-2021
Date: 2021-01-26
Publication information: BMJ Case Reports 2021; 14(1): e237860
Abstract: Salpingitis isthmica nodosa (SIN) is the nodular swelling or diverticulum of the isthmus of the fallopian tube. It is most commonly identified when investigating female infertility or in association with ruptured ectopic pregnancies. We experienced a rare and atypical presentation of SIN. A 33-year-old woman presented with a 1-hour history of acute lower abdominal pain associated with nausea and vomiting. CT and pelvic ultrasound revealed haemoperitoneum with no radiological evidence for its aetiology. Initial beta-human chorionic gonadotropin excluded ectopic pregnancy. A diagnostic laparoscopy was performed following clinical deterioration of the patient. Active bleeding of the right fallopian tube was identified and managed with a right partial salpingectomy, with subsequent histopathology revealing ruptured SIN. There have been no reported cases of SIN being a primary cause for an acute abdomen or haemoperitoneum in the absence of an ectopic pregnancy, making this case a surgical novelty.
URI: https://ahro.austin.org.au/austinjspui/handle/1/25746
DOI: 10.1136/bcr-2020-237860
ORCID: 0000-0002-8534-4237
0000-0001-5763-5742
Journal: BMJ Case Reports
PubMed URL: 33500302
Type: Journal Article
Subjects: general surgery
obstetrics and gynaecology
Appears in Collections:Journal articles

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