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| http://dx.doi.org/10.1007/s13224-021-01604-9 | DOI Listing |
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Charcot-Marie-Tooth Disease Presenting in the Postpartum Period: A Case Report.
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Clinical Neurophysiology, University Hospital of Wales, Cardiff, GBR.
Charcot-Marie-Tooth disease (CMT) is the most common hereditary peripheral neuropathy. It presents a wide range of genetic and phenotypic heterogeneity. CMT disease type 1A (CMT1A), caused by PMP22 gene duplication, represents the most common subtype of CMT in Western countries.
View Article and Find Full Text PDFHaematometra arising from multiple abortions: a comprehensive case report.
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Department of Obstetrics and Gynaecology, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon.
Haematometra, a rare and delayed complication, can emerge following medical termination of pregnancy, also known as 'postabortal post-caesarean syndrome' or 'redo syndrome'. Treatment requires the immediate evacuation of both liquid and clotted blood for quick resolution, followed by administration of an oxytocic agent to ensure complete recovery. This current report describes a female patient in her mid-30s who presented with colicky lower abdominal pain following a medically-induced abortion at 10 weeks.
View Article and Find Full Text PDFIsthmocele: A Case Report and Review of an Increasingly Common Gynecological Hurdle.
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Gynecologic Oncology, Wolverhampton Royal Hospital, Birmingham, GBR.
Isthmocele is emerging as an increasingly common yet troublesome diagnosis. The spectrum of potential symptoms is large, with subsequent management strategies continuing to evolve. For clinicians, having first recognized the inconsistencies in presentation, familiarity with the differing treatment options is important.
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Department of Medicine, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.
Introduction: Primary hyperparathyroidism (PHPT) during pregnancy is rare, with the commonest cause being parathyroid adenoma. Parathyroid cysts represent 0.5% of parathyroid lesions.
View Article and Find Full Text PDFSpontaneous ruptured pyomyoma: A rare yet critical postpartum complication: A case report.
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Medical Department, Klinik Kesihatan Bandar Baru Air Itam, Pulau Pinang, Ayer Itam 11500, Malaysia.
Pyomyoma, a rare complication of leiomyoma, presents a unique clinical challenge due to its infrequency with potentially fatal complications. Herein, we report the case of a 44-year-old Para 3+1 woman with red degeneration of uterine fibroids during pregnancy, who experienced worsening abdominal pain and foul smelling vaginal discharge 1 week post Caesarean section. Despite hemodynamic stability, her septic markers were markedly raised.
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