Results 71 to 80 of about 30,430 (219)

Early symptoms and sensations as predictors of lung cancer: a machine learning multivariate model. [PDF]

open access: yes, 2019
The aim of this study was to identify a combination of early predictive symptoms/sensations attributable to primary lung cancer (LC). An interactive e-questionnaire comprised of pre-diagnostic descriptors of first symptoms/sensations was administered to ...
Bernhardson, B-M.   +9 more
core   +1 more source

Cutaneous Ciliated Cyst of the Ear

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Cutaneous ciliated cysts are rare benign lesions initially observed exclusively in the lower extremities of young females. Since their first descriptions, there have been numerous case reports of the entity occurring in males and females, in varying anatomical locations. Here, we present a case of cutaneous ciliated cyst reported for the first
Allan Fong   +2 more
wiley   +1 more source

Hamartoma of parapharyngeal space: A rare case report

open access: yesMAMC Journal of Medical Sciences, 2016
A hamartoma is a tumor-like lesion made up of tissues indigenous to the part but lacks the true growth potential of a true neoplasm. Hamartomas are rare in head and neck region.
Swati Tandon   +3 more
doaj   +1 more source

A rare case of angiomyomatous hamartoma of periaortic lymph node and synchronous angiomyolipoma of the kidney: a diagnostic pitfall for lymph node involvement by angiomyolipoma

open access: yesHuman Pathology: Case Reports, 2020
Angiomyomatous hamartoma is a rare benign proliferative lesion of lymph nodes, showing replacement of the lymph node parenchyma by irregular thick-walled blood vessels, smooth muscle, fibrotic stroma and variable amount of adipose tissue.
Zsolt Jobbagy   +4 more
doaj   +1 more source

هامارتوم کندروييد قفسه سينه در نوزادی: گزارش يک مورد نادر [PDF]

open access: yes, 2010
مقدمه: هامارتوم کندروييد قفسه سينه، تومور خوش ­خيم بسيار نادری است که معمولاً هنگام تولد يا در ابتدای دوران کودکی بروز مي­يابد. اين بيماری غالباً به­صورت يک توده قابل لمس در جدار قفسه سينه تظاهر مي­يابد.
جهانگيری, فریبا   +3 more
core  

Diprosopus dirrhinus (nasal duplication) in a female Holstein Friesian calf: Clinical findings, diagnostic imaging and surgical management

open access: yesVeterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract An 11‐week‐old Holstein Friesian heifer calf presented with a congenital nasal abnormality characterised by an additional, turbinate‐like structure located dorsally on the nasal bridge. Clinical examination of the calf revealed normal respiratory function, with the accessory structure producing mucoid discharge from blind‐ended cavities ...
Raffaela Marian   +4 more
wiley   +1 more source

Kisspeptin as a test of hypothalamic dysfunction in pubertal and reproductive disorders

open access: yesAndrology, Volume 14, Issue 4, Page 1002-1016, May 2026.
Abstract The hypothalamic–pituitary–gonadal axis is regulated by the gonadotropin‐releasing hormone pulse generator in the hypothalamus. This is comprised of neurons that secrete kisspeptin in a pulsatile manner to stimulate the release of GnRH, and, in turn, downstream gonadotropins from the pituitary gland, and subsequently sex steroids and ...
Aureliane C. S. Pierret   +5 more
wiley   +1 more source

Acral Mesenchymal Spindle Cell Neoplasm With a Novel HMGA2::NCOA2 Fusion

open access: yesJournal of Cutaneous Pathology, Volume 53, Issue 5, Page 402-406, May 2026.
ABSTRACT Molecular profiling has revolutionized the field of soft tissue pathology, enhancing diagnostic precision and treatment strategies. The integration of molecular analysis and immunohistochemistry has been crucial for classifying diagnostically challenging acral mesenchymal neoplasms.
Grace Z. Armstrong   +5 more
wiley   +1 more source

Double‐chambered left ventricle in a pediatric patient with tuberous sclerosis complex: A case report

open access: yes
Pediatric Investigation, EarlyView.
Haoxuan Li   +6 more
wiley   +1 more source

Low‐Level Mosaicism in Tuberous Sclerosis Complex (TSC): Diagnostic and Clinical Implications From Two Novel Cases and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 862-870, April 2026.
ABSTRACT Mosaicism is relatively common in Tuberous Sclerosis Complex (TSC) but can be difficult to detect using routine diagnostic tests, particularly when the variant allele frequency (VAF) is low. We describe two cases of mosaic TSC diagnosed using an ultra‐deep sequencing approach in multiple tissues and review the literature about this topic in ...
Irene Ambrosetti   +14 more
wiley   +1 more source

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