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Nevus lipomatosus superficialis mimicking ectopic breast tissue: A rare case report.
Medicine (Baltimore)
February 2025
Department of Plastic and Reconstructive Surgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Rationale: Diagnosis of solitary superficial lipomatous mass may vary depending on circumstances. Although preliminary diagnosis can be made through clinical symptoms and imaging studies, final diagnosis can change through histological examination. This is the first reported case of nevus lipomatosus superficialis (NLS) resembling ectopic breast tissue which may provide valuable insights for clinicians managing similar lesions.
View Article and Find Full Text PDFLarge Nevus Lipomatosus Cutaneous Superficialis in the Skin of Color.
Skinmed
January 2025
Division of Dermatology, Department of Medicine, Albert Einstein College of Medicine, Montefiore Hospital, Bronx, NY.
A 15-year-old African-American man (Fitzpatrick skin type V) presented to the outpatient dermatology clinic with a large, verrucous, exophytic mass measuring 3.5 × 2.3 cm on the right lateral side of the posterior flank (Figure 1).
View Article and Find Full Text PDFReview of encephalocraniocutaneous lipomatosis.
Semin Pediatr Neurol
December 2024
Dell Medical School, The University of Texas at Austin, Austin, TX, USA. Electronic address:
Article Synopsis
- Encephalocraniocutaneous lipomatosis (ECCL), or Haberland syndrome, is a rare condition affecting the skin, central nervous system, and eyes, characterized by tumors and other abnormalities.
- Key symptoms include specific skin lesions, subcutaneous lipomas, and neurological issues like intracranial lipomas and developmental delays.
- Diagnosis primarily relies on clinical evaluation with possible genetic testing; management is multidisciplinary, focusing on symptom relief and monitoring for potential complications.
Giant Cerebriform Nevus Lipomatosus Cutaneous- Superficialis with Diffuse Lipomatosis: An Unusual Presentation on the Neck.
Skinmed
August 2024
Consultant Pathologist, Dr. Lal Path Labs, Bathinda, Punjab, India.
Article Synopsis
- * The swelling is described as a large, soft, yellowish to skin-colored mass with no tenderness or ulceration, and there are also small, soft papules around it.
- * Differential diagnoses for the swelling include plexiform neurofibroma and nevus lipomatosus cutaneous superficialis (NLCS).
SOLAMEN syndrome with cardiovascular damage.
Hereditas
July 2024
Department of Burn and Plastic Surgery, The Children's Hospital, National Clinical Research Center, Zhejiang University School of Medicine, Zhejiang Hangzhou, PR China.
Article Synopsis
- SOLAMEN syndrome is a rare congenital disorder marked by progressive, multi-system issues like overgrowth, lipomatosis, arteriovenous malformation (AVM), and epidermal nevus, primarily linked to a PTEN gene mutation.
- The syndrome’s symptoms can overlap with other conditions, making diagnosis tricky and often leading to misdiagnoses such as Klippel-Trenaunay or Parks-Weber syndromes.
- A specific case of a child with various symptoms including macrocephaly and significant AVM was documented; genetic sequencing confirmed a PTEN mutation and highlighted the need for regular health evaluations and potential treatments due to the risk of AVM progression and cardiac defects.
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