Eosinophilic fasciitis is a rare disease characterized by diffuse fasciitis with peripheral eosinophilia and progressive induration and thickening of the skin and soft tissues. We report a 19-year-old female who presented with pitting edema in both lower extremities. She had a history of excessive physical activity before her symptoms developed. Physical examination revealed 2+ pitting edema in both lower legs. She complained of mild pain in both knee joints and feet, with no tenderness or heating sensations. Laboratory results were unremarkable except for severe eosinophilia. Parasite infection, venous thrombosis, and cardiac and renal problems were excluded. A magnetic resonance imaging study of both lower extremities revealed increased signal intensity in the subcutaneous lesions, consistent with superficial inflammation of the fascia. Mixed perivenular lymphoplasmacytic and eosinophilic infiltration in the subcutaneous lesion were observed on biopsy. The patient was treated with corticosteroids, resulting in remarkable improvement in both edema and eosinophilia.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936049PMC
http://dx.doi.org/10.4168/aair.2014.6.2.179DOI Listing

Publication Analysis

Top Keywords

pitting edema
12
edema lower
12
lower extremities
12
eosinophilic fasciitis
8
case eosinophilic
4
fasciitis presenting
4
presenting pitting
4
edema
4
lower
4
extremities eosinophilic
4

Similar Publications

Pregnancy-Related Morphea: A Case Report.

Clin Med Insights Case Rep

December 2024

Department of Obstetrics and Gynecology, School of Medicine, Reproductive Health Research Center, Guilan University of Medical Sciences, Rasht, Iran.

Background: Morphea is a skin condition marked by erythematous and hardened inflammatory lesions that can progress to atrophic and sclerotic plaques. In this case report, we present a case of a pregnant woman who showed morphea presentation.

Case Presentation: A 37-year-old GPL woman with a gestational age of 32 weeks and 2 days was referred to the hospital with complaints of swelling, pain, and erythema in both legs for the past week, without any obstetric complaints.

View Article and Find Full Text PDF

Background: Large-for-size syndrome (LFSS) is an uncommon but potentially lethal complication following adult liver transplantation (LT). Reduced-size liver transplantation (RSLT) is considered a valuable alternative to delayed fascial closure or mesh closure for preventing LFSS. In this article, we report a successful adult-to-adult RSLT case with right posterior graft sectionectomy using three-dimensional (3D) computer-assisted planning.

View Article and Find Full Text PDF

Diffuse alveolar hemorrhage (DAH) is a rare but severe pulmonary complication in systemic lupus erythematosus (SLE), characterized by alveolar bleeding leading to respiratory distress, hypoxemia, and often hemoptysis. Rapid diagnosis and aggressive immunosuppressive therapy are crucial for survival. A 55-year-old woman with a five-year history of SLE presented with acute dyspnea, hemoptysis, pleuritic chest pain, fatigue, and low-grade fever.

View Article and Find Full Text PDF

Hereditary angioedema in children: Review and practical perspective for clinical management.

Pediatr 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.

View Article and Find Full Text PDF
Article Synopsis
  • Myocardial dissection is a rare but serious complication of ischaemic heart disease, characterized by a haematoma forming within the cardiac muscle, often triggered by factors such as increased wall tension and reduced tensile strength.
  • A case study highlights a 37-year-old male, who developed myocardial dissection following an ST elevation infarction after years of substance abuse, including heroin and methamphetamines, which might be linked to his condition.
  • The patient presented with symptoms of heart failure, and diagnostic tests revealed severe heart dysfunction and a mass in the heart, leading to treatment with diuretics and medical therapy instead of surgery due to high operative risk.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!