Results 41 to 50 of about 55,987 (150)
An Update on the Ophthalmologic Features in the Phakomatoses
Journal of Ophthalmology, Volume 2016, Issue 1, 2016., 2016 Neurofibromatosis type 1, tuberous sclerosis complex, and Von Hippel‐Lindau disease, historically classified as the phakomatoses, are hereditary multisystem disorders characterized by the presence of hamartoma, which carry the risk of malignant transformation. The alteration of tumor suppressor genes seems to be at the basis of their pathophysiogenetic
Solmaz Abdolrahimzadeh +4 more
wiley +1 more source
Immunohistochemical characterization of the 'intimal proliferation' phenomenon in Sneddon's syndrome and essential thrombocythaemia [PDF]
, 1994 Cellular changes were immunocytochemically characterized in skin vessels of five patients with idiopathic generalized racemose livedo (Sneddon's syndrome), and one patient with localized racemose livedo associated with essential thrombocythaemia ...
Wolter, M. +3 more
core +1 more source
Adult Occipital Dermoid Cyst With the Initial Manifestation of Subcutaneous Lump: A Case Report
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT Dermoid cysts require meticulous differential diagnosis, prompt surgical intervention, proactive management of infection and other complications, precise delineation of the lesion prior to operation, and efforts to achieve complete excision. We report a case initially diagnosed as an epidermoid cyst but finally confirmed as a dermoid cyst.
Tingting Zhong +4 more
wiley +1 more source
European Journal of Neurology, Volume 33, Issue 2, February 2026.Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley +1 more source
Respirology Case Reports, Volume 13, Issue 11, November 2025.Bronchial artery‐pulmonary artery fistula (BPAF) with dual arterial feeders is a rare vascular anomaly with the potential risk of catastrophic rupture. Our case report demonstrated the role of endovascular embolisation in preventing massive life‐threatening haemorrhage.
Hei‐Shun Cheng +9 more
wiley +1 more source
Cysts and tumours of the iris: Diagnostic tools and key management considerations—A review
Clinical &Experimental Ophthalmology, Volume 52, Issue 6, Page 665-683, August 2024.Abstract The iris is a unique structure, with exquisite variations in colour and form. Pathological changes, specifically including iris cysts and tumours are relatively uncommon, difficult to diagnose, and yet potentially blinding or life‐threatening.
Bia Z. Kim +2 more
wiley +1 more source
Cardiac hemangioma of the right atrium in a neonate : fetal management and expedited surgical resection [PDF]
, 2005 Cardiac hemangioma is a rare tumor with a reported incidence of 1-2%. We describe the case of a neonate with a right atrial mass that was diagnosed prenatally. The fetus developed a supraventricular tachycardia and was delivered by cesarean section in
Campbell, A. +5 more
core
Laser Photocoagulation of Tongue Hemangioma: Case Report [PDF]
, 2013 This report describes two cases of tongue hemangioma and shows the effectiveness of photocoagulation with diode laser. A thirty-five year-old female patient with a tongue hemangioma measuring 20x30 mm was referred.
Remzi Doğan +4 more
core +1 more source
Racemose hemangioma (a case from practice)
Russian Pediatric Ophthalmology, 2011 The authors described a case of racemose hemangioma of the retina in combination with malformations of orbital vessels. In spite of congenital character of the pathology, decrease of the central vision appeared at the age of 25.
Ol'ga Vladimirovna Paramey +7 more
openaire +1 more source