Lipomas are among the most common tumors seen in the soft body parts and usually are solitary lesions. The authors report a case of a male patient that presented for evaluation of multiple subcutaneous nodules that caused important functional and cosmetic impairment. The diagnosis of familial multiple lipomatosis was made. Physicians should be able to recognize and characterize this rare disease.
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http://dx.doi.org/10.1590/s0365-05962012000200027 | DOI Listing |
Ann Endocrinol (Paris)
December 2024
GCS AURAGEN, 69003 Lyon, France.
We describe for the first time the case of a woman presenting with Tatton-Brown-Rahman syndrome (TBRS) and multiple endocrine neoplasia (MEN). She developed primary hyperparathyroidism at age 13, a pituitary cyst at age 14, adrenal tumor at age 21, and metastatic insulinoma at age 34. In addition, she showed intellectual disability, obesity, multiple lipomas, facial dysmorphia, hemihypertrophy and kyphoscoliosis.
View Article and Find Full Text PDFJ Ultrason
December 2024
Department of Diagnostic Imaging and Interventional Radiology, Pomeranian Medical University, Szczecin, Poland.
The aim of this paper is to present our experience in transabdominal ultrasonography of ileocecal valve lesions. The ileocecal valve, located in the central part of the ileocecal bowel segment, is rarely the primary site of disease processes. It is usually involved by pathologies in adjacent bowel segments.
View Article and Find Full Text PDFJ Hand Surg Eur Vol
December 2024
Department of Hand Surgery, Fremantle Hospital, Western Australia, Australia.
Intraneural lipomas and lipofibromas are rare, benign median nerve tumours. We report a 62-year-old woman with carpal tunnel syndrome owing to an intraneural lipoma. MRI is the reference standard investigation for diagnosis, directing treatment towards operative or non-operative management.
View Article and Find Full Text PDFJ Med Case Rep
December 2024
Department of Pulmonology, Pius-Hospital Carl Von Ossietzky University, Oldenburg, Germany.
Background: Yellow nail syndrome is characterized by a yellow discoloration of the nails, respiratory symptoms, and lymphedema. It was first described in 1964 and has an estimated prevalence of less than 1:1.000.
View Article and Find Full Text PDFRadiol Case Rep
January 2025
Radiology Department, University Hospital Souss Massa, Faculty of Medicine and Pharmacy, Ibn Zohr University, Agadir, Morocco.
Tethered cord syndrome is a rare form of spinal dysraphism. We present the case of a 24-year-old female patient who was admitted with chronic urinary symptoms, including dysuria and pollakiuria, which had persisted since puberty, along with lower back pain (lumbago). Due to the progression and increased severity of the lumbago, a lumbar MRI was performed.
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