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Ossifying fibromyxoid tumours with lipomatous and cartilaginous differentiation: A diagnostic pitfall.
Histopathology
December 2024
Department of Pathology and Laboratory Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Aims: Ossifying fibromyxoid tumour is a rare mesenchymal neoplasm predominantly affecting adults characterised by a multinodular growth pattern and the presence of a fibrous pseudocapsule with areas of ossification. Prompted by the recognition of a non-ossifying ossifying fibromyxoid tumour with lipomatous differentiation which caused diagnostic difficulty, we sought to further explore cases of ossifying fibromyxoid tumour with non-osseous heterologous elements.
Methods And Results: A search of our institutional and consultation archives revealed three additional cases that demonstrated lipomatous components and two cases with cartilaginous differentiation.
Review 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.
Case report: A challenging case of mixed-variant myofibroblastoma with complex imaging and pathological diagnosis.
Front Oncol
October 2024
Department of Orthopaedic Oncology & Surgery, Saitama Medical University International Medical Center, Saitama, Japan.
Myofibroblastomas are benign mesenchymal tumors that frequently occur in the groin. They show variable morphology, and the differential histopathological diagnoses are broad, including lipomatous to myxoid tumors. In addition, both pathological and imaging findings may be complex, which makes diagnosis challenging.
View Article and Find Full Text PDFSOLAMEN 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.
Immunohistochemical characteristics of uterine lipoleiomyomas.
Pathol Res Pract
August 2024
Pathology Department, University Hospital of Saint-Etienne, Saint-Etienne, France.
Lipoleiomyomas are rare variants of uterine leiomyomas rarely studied in the literature. We retrospectively studied 20 cases of uterine lipoleiomyomas showing that these lesions represent 0.7 % of all uterine leiomyomas diagnosed histologically.
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