Imaging manifestations of juvenile hyaline fibromatosis: A case report and literature review

Objective: Juvenile hyaline fibromatosis (JHF) is an autosomal recessive condition caused by a mutation in capillary morphogenesis gene 2 (CMG2) on chromosome 4q21. JHF is an extremely rare genetic disorder, and fewer than a hundred cases have been reported worldwide. In this case report, the clinical features, histopathological features and imaging manifestations of a case of JHF are presented. We present imaging manifestations of one case of JHF to deepen the radiologist’s understanding of this condition. The histopathological feature of JHF is hyaline degeneration involving skeletal muscle. Therefore, the lesion has a slightly high density on CT imaging, iso- or hypointense signal on T1WI and hypointense signal on T2WI. The boundary between the lesion and skeletal muscle is unclear. Methods: An 8-year-old male (case 1) was examined in our department with a complaint of multiple masses on the head, neck and back in 2021. The boy was the only child of his parents and was delivered at 40 weeks gestation by caesarean section. His parents were nonconsanguineous. Results : JHF displays multiple slowly or rapidly growing subcutaneous nodules. The imaging manifestations can reflect histopathological components, including nodular connective tissue and amorphous, partially calcified hyaline material.

Dermoscopy of pilomatricoma: A case report with a review of the literature

Pilomatricoma is a benign tumor originating from hair follicle matrix cells and characterized by the presence of cutaneous and subcutaneous nodules up to 3.0 cm in diameter, usually on the head, neck, and upper extremities, rarely on the trunk and lower extremities. An eleven-year-old female with a painless, erythematous-purplish tumor of the back. A dermoscopic examination revealed irregular linear vessels, white structures, and structureless grayish-blue areas. Histological examination after excision confirmed the diagnosis of pilomatricoma. Dermoscopy may be a useful tool for improving the clinical recognition of pilomatricoma.

Evaluation of Working Conditions as a Factor of Well-Being of Workers in an Electronic Industry in Mexicali

The objective of this research was developed to evaluate the working conditions of workers in an electronic industry located in the city of Mexicali, analyzing a process in a work table where welding operations of electronic components are made and certain factors are presented that generated discomfort to the operating personnel of this manufacturing area. The workers frequently visited the company doctor and health institutions in Mexicali due to symptoms of discomfort and pain in the head, neck, back, spine, arms, hands, and shoulders in addition to discomfort in the eyes due to not having a position due to poor structure (work table and chair) and low light intensity, which caused fatigue and stress and discomfort with eyestrain. In addition, certain employees in the production areas presented symptoms of respiratory diseases caused by an environment contaminated by pollutants, essentially derived from sulfur (sulfides), as well as variations in temperature and relative humidity in the four seasons of the year.

Masson’s Tumour: A Rare Cause of Cervical Mass

Masson's tumour, also known as intravascular papillary endothelial hyperplasia, is a rare non-neoplastic lesion of vascular origin, caused by an excessive reactive proliferation of endothelial cells in normal blood vessels or vascular malformations. It can affect any part of the body, presenting most frequently in the vessels of the head, neck and upper extremities. The authors describe the case of a 76-year-old female patient presenting an anterior cervical mass, measuring 2×2 cm, which was mobile, tender and slightly painful with no alteration of the overlying skin. Complementary study with ultrasound and computed tomography was inconclusive. Total excision of the lesion was performed with histology compatible with intravascular papillary endothelial hyperplasia.