Genital oedema of primary and secondary aetiology is gaining increased recognition; it occurs in people of all ages, although accurate prevalence remains unknown. While reports of surgical intervention are quite common, clear description of conservative management is rare, and, overall, diagnosis and management remain largely delayed. Conservative management of genital oedema requires imaginative use of compression bandages and support garments, adapted manual lymphatic drainage, enablement of exercise and activities required for school/employment and diligent skin care to avoid cellulitis. The aim of this article is to present case reports from two European countries discussing five males of differing ages and with genital oedema of different aetiology as examples of conservative management of male genital oedema. The case reports include an adolescent boy with genital oedema since age 1 year, a 49-year-old man treated for penile cancer, a 60-year-old man treated for primary rectal lymphoma, a 48-year-old man with morbid obesity and a 49-year-old with obesity and recurrent infections. The latter two cases integrate surgery and conservative care. Case reports can be a useful means of addressing education needs related to rarer conditions and sharing practice where diagnostic criteria and specific protocols of care are lacking.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.12968/jowc.2021.30.Sup12a.6 | DOI Listing |
BMJ Case Rep
December 2024
Department of Surgery, Post Graduate Institute of Medical Education and Research and Capital Hospital, Bhubaneswar, Odisha, India
Spontaneous transvaginal small bowel evisceration, without recent trauma or surgery, is extremely rare. Complications include bowel obstruction, perforation, gangrene, septicaemia and death, requiring urgent surgical intervention. We report a case of a woman in her late 60s, who presented with 70-75 cm of small intestine eviscerated through the vagina, alongside a long history of uterine and rectal prolapse.
View Article and Find Full Text PDFPediatr Allergy Immunol
December 2024
French National Reference Center for Angioedema (CREAK), Center of Excellence and Reference (ACARE), Internal Medicine Department, Grenoble Alpes University Hospital, Grenoble, France.
Background: Hereditary angioedema (HAE) in children has specific features and requires multidisciplinary management.
Methods: We performed a literature search and underwent in-depth discussions to provide practical tools for physicians.
Results: HAE is a rare, life-threatening genetic disorder.
Aktuelle Urol
December 2024
Klinik für Urologie, Kinderurologie und roboterassistierte minimalinvasive Urologie, Sozialstiftung Bamberg, Bamberg, Germany.
Enormous oedema of the male genitals, such as penoscrotal elephantiasis, is a very rare condition. It is usually a result of recurrent inflammation, trauma or malignancy, although the main cause is lymphatic filariasis. Furthermore, it is a challenging condition for both patient as well as the attending healthcare team.
View Article and Find Full Text PDFOxf Med Case Reports
November 2024
Faculty of Medicine, Palestine Polytechnic University, Hebron 9020000, Palestine.
Behçet's disease (BD) is characterized by skin lesions, uveitis, and recurrent oral and genital ulcers. Vascular problems, predominantly affecting veins, lead to thrombosis, increasing the risk of ruptured artery aneurysms and Budd-Chiari syndrome (BCS). Morbidity and mortality are significantly heightened by rare occurrences such as pulmonary artery aneurysms, cardiac involvement, and BCS.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!