Results 21 to 30 of about 5,256 (198)

Diffuse skeletal angiomatosis.

Italian journal of orthopaedics and traumatology, 1981
Diffuse skeletal angiomatosis is a very rare syndrome. Since it was first observed by Shennan in 1915 only fifty-five cases have been reported in the literature (Rondier et al., 1977). It therefore seems that the description of a new case, accompanied for the first time by ultrastructural findings, may offer a new insight into the pathology of this ...
FERRETTI, Andrea, R. Sadun, G. Gherardi
openaire   +3 more sources

Cutaneous reactive angiomatosis with combined histological pattern mimicking a cellulitis [PDF]

, 2013
Cutaneous reactive angiomatoses (CRA) encompass a distinct group of rare benign reactive vascular proliferations that include reactive angioendotheliomatosis, diffuse dermal angiomatosis and reactive intralymphatic histiocytosis.
Beltraminelli, H., Corti, Michela AngelaMaria, Corti, M. A. M., Rongioletti, F., Borradori, Luca, Beltraminelli, Helmut, Borradori, L., RONGIOLETTI, FRANCO   +7 more
core   +4 more sources

Perioperative Challenges in a Patient With Sturge-Weber and Obesity Hypoventilation Syndromes. [PDF]

Case Rep Med
Background The rare concurrence of Sturge–Weber syndrome (SWS) and obesity hypoventilation syndrome (OHS) presents significant anesthetic challenges, with complexity in airway management and perioperative respiratory care. Case Presentation A 55‐year‐old man with SWS and OHS underwent elective dental extraction.
Mincolelli G, Izzi A, Leoni MLG, Marchello V, Carlo MGD, Cascella M, Recchia A, Corso RM.   +7 more
europepmc   +2 more sources

Bacillary angiomatosis in HIV-infected patients - An epidemiological and clinical study [PDF]

, 2000
Background: No data were available on the epidemiological and clinical characteristics of bacillary angiomatosis (BA) in Germany. Objective:To determine epidemiological and clinical data on HIV-associated BA.
Rasokat, H., Bogner, Johannes R., Kaliebe, T., Plettenberg, Andreas, Albrecht, H., Schöfer, H., Mertenskötter, T., Lorenzen, T., Burtsche, B. T., Stoehr, A.   +9 more
core   +1 more source

Adhesion and host cell modulation: critical pathogenicity determinants of Bartonella henselae [PDF]

, 2011
Bartonella henselae, the agent of cat scratch disease and the vasculoproliferative disorders bacillary angiomatosis and peliosis hepatis, contains to date two groups of described pathogenicity factors: adhesins and type IV secretion systems.
Kempf Volkhard AJ, Volkhard AJ Kempf, Kempf, Volkhard A. J., Bettina Franz, Franz, Bettina, Franz Bettina   +5 more
core   +1 more source

Impact of Periodontal Therapy in Patients with Sturge-Weber Syndrome [PDF]

Journal of Clinical and Diagnostic Research, 2019
A 19 years old female patient, presented with the chief complaint of pain and swelling on her face. At physical examination, facial asymmetry and “port wine” spots on the left face were seen.
Iasminy Soares De Oliveira, Teresa Cristina Esteves, André Caroli Rocha, Maria das Graças Afonso Miranda Chaves, Gisele Maria Campos Fabri   +4 more
doaj   +1 more source

Plausible predicament in emergency endodontic rehabilitation of a child with Sturge-Weber syndrome: A case report

Contemporary Pediatric Dentistry, 2022
Sturge–Weber Syndrome (SWS) is a neuro-oculo-cutaneous vascular disorder that includes leptomeningeal hemangioma and port wine stains, usually ipsilaterally, with ocular manifestations and extended lesions over the oral cavity.
Amit Khatri, Namita Kalra, Rishi Tyagi, Khadeeja Kulood M, Mayank Sharma, Drishti Kaushal   +5 more
doaj   +1 more source

Vertebral Angiomatosis in a Persian cat

, 2014
This report describes a case of a young Persian cat with vertebral angiomatosis. The patient initially presented for evaluation of lethargy, inappetance, and non-specific pain.
Gambino, Stephanie
core   +4 more sources

Gorham Stout syndrome in a pediatric patient. A case report

Medisur, 2023
Within the idiopathic osteolysis syndromes classification, Gorham-Stout disease ranks fourth. It is a clinical picture characterized by the progressive destruction of bone tissue and vascular proliferation, with angiomatosis and bone lymphangiomatosis ...
Ariel Moya Machado, Leidelén Esquivel Sosa, Yisel González Ríos   +2 more
doaj  

Bloom Syndrome Presenting With Early-Onset Myelodysplastic Syndrome and Triple Overlapping Vascular Neurocutaneous Phenotypes: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Bloom syndrome is a rare autosomal recessive chromosomal instability disorder characterized by growth deficiency and early‐onset malignancies, and its coexistence with multiple vascular neurocutaneous syndromes is exceptionally uncommon. We report an 8‐year‐old girl who presented with severe growth failure and persistent pancytopenia.
Shahgholi E, Khosroshahi N, Sadeghi S.
europepmc   +2 more sources