Results 101 to 110 of about 57,842 (313)
World Journal of Surgical Oncology, 2014 BackgroundNasal chondromesenchymal hamartoma (NCMH) is an extremely rare benign tumor, primarily diagnosed in young infants and children and it often simulates malignant tumors on imaging.Case presentationWe present computerized tomography and magnetic ...
Tingting Wang +7 more
semanticscholar +1 more source
Multidisciplinary surgical management of Cowden syndrome: report of a case [PDF]
, 2016 Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000 patients with an incomplete penetrance and variable expressivity, characterized by alterations in a tumor suppressor gene. A 14-year-old Caucasian male
Gallenzi, Patrizia +2 more
core +1 more source
Cancer Medicine, Volume 15, Issue 2, February 2026.Encouraging survival is achieved in phakomatosis syndromes with conventional multimodality treatment (Surgery, RT, chemotherapy). There is an urgent need for easily administered systemic therapies which improve both quality and quantity of life. ABSTRACT Purpose Phakomatoses‐associated primary central nervous system (CNS) tumors are therapeutically ...
Anuradha Krishnan +10 more
wiley +1 more source
Classification of hypothalamic hamartoma and prognostic factors for surgical outcome
Acta Neurologica Scandinavica, 2014 The main aims of this study were to classify patients with hypothalamic hamartoma (HH) based on neuroimaging features and describe the clinical manifestations of HH.
C. D. Li +5 more
semanticscholar +1 more source
, 2011 Bacground. Gastric adenomyoma is a rare, hamartomatous tumor localized most frequently in the gastric antrum. Review of the available literature shows only sporadic reports or smaller series. Case reports. We presented a 72-year-old woman admitted due
Ignjatović Igor I. +6 more
core +1 more source
Undifferentiated Embryonal Sarcoma of the Liver in a 6 Years Old Male Patient: A Case Report
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Undifferentiated Embryonal Sarcoma of the Liver (UESL) is a rare, aggressive mesenchymal tumor predominantly affecting children. Its non‐specific clinical presentation and variable imaging characteristics often lead to diagnostic delays and complex management.
Rajab Msemo +5 more
wiley +1 more source
Case Reports in Pathology, 2015 We report a case of pancreatic hamartoma-like solitary fibrous tumor which was differentiated from pancreatic hamartoma with the detection of NAB2-STAT6 fusion, a specific mutation for solitary fibrous tumors.
Kei Tanaka +4 more
doaj +1 more source
Central precocious puberty in a 3 year-old girl with Phenylketonuria: a rare association? [PDF]
, 2014 Background Central precocious puberty (CPP) and phenylketonuria (PKU) are two rare conditions, the latter being the rarer. To date, only one case featuring both these conditions has been reported, and hyperphenylalaninemia was assumed triggering CPP.
Donaldson, Malcolm +3 more
core +3 more sources
Respirology Case Reports, Volume 14, Issue 2, February 2026.Accurate localisation of small or non‐palpable pulmonary lesions is critical for successful minimally invasive resection. We present a four‐patient case series—the first in Germany—where ICG‐soaked embolisation coils were placed using ultrathin bronchoscopy, a standard cytology brush catheter and cone beam CT (CBCT) guidance, without robotic ...
Sammy Onyancha +6 more
wiley +1 more source
Journal of Medical Case ReportsBackground We present this case to highlight the importance of considering seromucinous hamartoma in the differential diagnosis of nasal cavity lesions, particularly due to its rarity and potential for being mistaken for more aggressive pathologies ...
Mikhael Makhoul +3 more
doaj +1 more source