Results 121 to 130 of about 298,062 (215)
Central Hemangioma of Mandible: Rare Case
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Central hemangioma, though it is a rare entity, should always be considered in the differential diagnosis of intraosseous radiolucent lesions, especially in younger patients, as missed diagnosis can lead to profuse intraoperative bleeding and pose life‐threatening complications. Comprehensive radiographic assessment and confirmatory biopsy are
Rakshya Shrestha +4 more
wiley +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Tuberous sclerosis complex (TSC) is a rare and complex autosomal dominant disease. Many patients with TSC may remain undiagnosed for years due to its widespread and heterogeneous clinical presentation, with only 1% of TSC patients developing end‐stage renal disease (ESRD).
Changlin Wei +5 more
wiley +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.A term newborn with nasal mass caused by choristoma (hairy poly). ABSTRACT We describe the case of a term Hispanic male neonate with a nasal septum/inferior turbinate choristoma. The presented case report includes a review of the historical, radiological, surgical, and histological features, and the literature on this entity.
Surasak Puvabanditsin +6 more
wiley +1 more source
Fabry Disease Associated With Myelodysplastic Syndrome: Case Report
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT This is the first reported case of Fabry disease (FD) coexisting with myelodysplastic syndrome (MDS). While the coexistence of FD and MDS may be incidental, the case underscores the importance of considering FD in patients with unexplained systemic and hematological abnormalities, particularly those with a family history.
Liping Zheng +5 more
wiley +1 more source
Thoracoscopic Management of Fibrous Dysplasia: First Experience in Turkey
Sakarya Tıp Dergisi, 2015 Fibrous dysplasia is a osseous pathology and bone structure is replaced by fibro-osseous tissue. Our patient was a 36-year-old female with a complaint of swelling on the right side of chest for seven years.
Ali Ulaş +4 more
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Fibrous Dysplasia of Bone and McCune–Albright Syndrome: A Bench to Bedside Review
Calcified Tissue International, 2019 Iris R. Hartley +3 more
semanticscholar +1 more source
An Unusual Case of Periapical Cemento‐Osseous Dysplasia
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Periapical cemento‐osseous dysplasia (PCOD) is a benign fibro‐osseous condition often discovered incidentally during radiographic examinations. Accurate diagnosis is crucial to prevent unnecessary treatment. Conservative management with regular monitoring is typically sufficient, as illustrated in this case involving a 62‐year‐old female ...
Emanuel Harouni +2 more
wiley +1 more source
Central and Peripheral Mechanisms of Low Exercise Capacity in Prematurely Born Adults
Comprehensive Physiology, Volume 15, Issue 5, October 2025.The lower exercise capacity described in preterm born adults is associated with impaired stroke volume augmentation in response to incremental exercise intensity, thus to a lower cardiac output response to exercise, compared to age‐matched individuals born at term.
Giorgio Manferdelli +6 more
wiley +1 more source
Diabetes/Metabolism Research and Reviews, Volume 41, Issue 7, October 2025.ABSTRACT Background In older adults, obesity is associated with frailty, conditions worsened by age related decline in bone mineral density (BMD) and muscle mass. Objective To evaluate whether a 3‐month Fibre‐Enriched High Carbohydrate (FEHC) diet preserves bone health, reduces inflammation and modulates Wnt signalling in older adults with obesity ...
Francesca Cannata +16 more
wiley +1 more source
Marfan syndrome with multiseptate pneumothorax and mandibular fibrous dysplasia
Lung India, 2009 We describe a rare case of pneumothorax due to Marfan syndrome associated with fibrous dysplasia of the mandible. Marfan syndrome and fibrous dysplasia were possibly due to a common etiological factor.
Kate A, Gothi D, Joshi J
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