Encysted hydroceles are often considered rare. We report three cases of Ghanaian boys who presented with left scrotal swellings at a primary care center. This paper emphasizes the importance of primary care practitioners considering a possible clinical diagnosis of encysted spermatic cord hydroceles in new-onset scrotal swellings in children and adolescents, as such cases may not be as rare as previously thought.

Keywords:Scrotal Hydrocelesg; Surgery; Primary Care; Ghana.

Abstract

Isolated tubal torsion is a rare diagnosis that can be easily missed due to nonspecific clinical and imaging features. To diagnose preoperatively, a high level of suspicion is required for this condition. We present a case where ultrasonography initially indicated salpingitis, but intraoperatively revealed tubal torsion with an interesting etiology.

Keywords:Sterilization; Tubal; Ovarian Torsion; Adnexa Uteri.

Mucormycosis is a rare and opportunistic fungal infection caused by the order Mucorales. The emergence of COVID-19 has led to a resurgence of this opportunistic infection. COVID-19 and its management protocols have been implicated in causing this surge due to sequential impaired immunity in affected patients. A high index of suspicion, along with prompt evaluation and management, is advisable for the best clinical outcome.

Keywords:COVID-19; Mucormycosis, Gastrointestinal.

Carnitine-acylcarnitine translocase deficiency with SLC25A20 c.199-10T>G variation is a rare condition, typically associated with severe neonatal outcomes. Recently, preimplantation genetic testing (PGT) has emerged as a screening test applicable to embryos produced through in vitro fertilization for genetic analysis before transfer. Thus, PGT allows for the identification and elimination of embryos carrying inherited genetic diseases. This case report aims to present data from PGT on intervention in the management of SLC25A20 c.199-10T>G variation, particularly in middle-income countries. A 26-year-old woman with a high-risk term pregnancy and a history of two sudden neonatal deaths underwent parental carrier testing, revealing heterozygous SLC25A20 c.199-10T>G variation in both parents. The subsequent pregnancy, identified as a homozygous for SLC25A20 c.199-10T>G mutation, was terminated at 20 weeks. The current pregnancy was successfully managed by in vitro fertilization-selective embryo transfer. Carnitine-acylcarnitine translocase deficiency owing to SLC25A20 c.199-10T>G variation can result in sudden neonatal collapse. Obstetricians should maintain a high index of suspicion in recurrent cases of unexplained early neonatal death. Parental carrier testing is crucial for prenatal management, and selective embryo transfer is a core treatment for heterozygous SLC25A20 gene carriers in this highly lethal disorder.

Keywords:Carnitine-acylcarnitine translocase; Pregnancy, High-Risk; Perinatal Death; Preimplantation Diagnosis; SLC25A20 Protein, Human; Fertilization in Vitro.