keyword
https://read.qxmd.com/read/38616844/penile-epithelioid-hemangioendothelioma-in-a-child
#21
Palak Singhai, Nitin James Peters, Aravind Sekar, Girdhar S Bora, Ujjwal Gorsi, Jai Kumar Mahajan
An 8-year-old boy initially thought to have a penile arteriovenous malformation was later diagnosed with a rare vascular sarcoma, epithelioid hemangioendothelioma (EHE). Despite challenges in diagnosis, he underwent supraselective angioembolization and partial penectomy for oncological clearance. EHE, a low-grade malignancy, requires prompt identification and treatment due to potential systemic involvement.
2024: Journal of Indian Association of Pediatric Surgeons
https://read.qxmd.com/read/38614921/timing-incidence-and-management-of-delayed-bleeding-after-partial-nephrectomy-in-patients-at-risk-for-recurrent-bilateral-multifocal-renal-tumors
#22
JOURNAL ARTICLE
Patrick T Gomella, Julie Solomon, Michael Ahdoot, Sandeep Gurram, Amir H Lebastchi, Elliot Levy, Venkatesh Krishnasamy, Michael T Kassin, Richard Chang, Bradford J Wood, W Marston Linehan, Mark W Ball
INTRODUCTION: Delayed bleeding is a potentially serious complication after partial nephrectomy (PN), with reported rates of 1%-2%. Patients with multiple renal tumors, including those with hereditary forms of kidney cancer, are often managed with resection of multiple tumors in a single kidney which may increase the risk of delayed bleeding, though outcomes have not previously been reported specifically in this population. The objective of this study was to evaluate the incidence and timing of delayed bleeding as well as the impact of intervention on renal functional outcomes in a cohort primarily made up of patients at risk for bilateral, multifocal renal tumors...
April 12, 2024: Urologic Oncology
https://read.qxmd.com/read/38614896/management-of-sporadic-intracranial-vascular-malformations-in-pregnancy-a-retrospective-analysis
#23
JOURNAL ARTICLE
S J Ellwood, A A Mootz, J M Carabuena, M K Farber, S C Reale
BACKGROUND: Sporadic intracranial vascular malformations can pose significant risk to parturients, and additional reports of management may inform patient care. Here we describe the peripartum management of parturients with intracranial vascular malformations. METHODS: After Institutional Review Board approval, we performed a retrospective analysis of parturients with a known sporadic intracranial vascular malformation including cavernous malformation, developmental venous anomaly, or arteriovenous malformation who delivered at our institution between 2007 and 2020...
March 19, 2024: International Journal of Obstetric Anesthesia
https://read.qxmd.com/read/38612762/molecular-and-cellular-characterization-of-primary-endothelial-cells-from-a-familial-cavernomatosis-patient
#24
JOURNAL ARTICLE
Laura Lorente-Herraiz, Angel M Cuesta, Jaime Granado, Lucía Recio-Poveda, Luisa-María Botella, Virginia Albiñana
Cerebral cavernous malformation (CCM) or familial cavernomatosis is a rare, autosomal dominant, inherited disease characterized by the presence of vascular malformations consisting of blood vessels with an abnormal structure in the form of clusters. Based on the altered gene ( CCM1/Krit1 , CCM2 , CCM3 ) and its origin (spontaneous or familial), different types of this disease can be found. In this work we have isolated and cultivated primary endothelial cells (ECs) from peripheral blood of a type 1 CCM patient...
April 2, 2024: International Journal of Molecular Sciences
https://read.qxmd.com/read/38608292/machine-learning-for-enhanced-prognostication-predicting-30-day-outcomes-following-posterior-fossa-decompression-surgery-for-chiari-malformation-type-i-in-a-pediatric-cohort
#25
JOURNAL ARTICLE
Victor Gabriel El-Hajj, Abdul Karim Ghaith, Adrian Elmi-Terander, Edward S Ahn, David J Daniels, Mohamad Bydon
OBJECTIVE: Chiari malformation type I (CM-I) is a congenital disorder occurring in 0.1% of the population. In symptomatic cases, surgery with posterior fossa decompression (PFD) is the treatment of choice. Surgery is, however, associated with peri- and postoperative complications that may require readmission or renewed surgical intervention. Given the associated financial costs and the impact on patients' well-being, there is a need for predictive tools that can assess the likelihood of such adverse events...
April 12, 2024: Journal of Neurosurgery. Pediatrics
https://read.qxmd.com/read/38608129/24-year-old-patient-with-klippel-trenaunay-syndrome-underwent-cementless-robotic-cruciate-retaining-tka-a-case-report
#26
JOURNAL ARTICLE
Landon Reading, Colin Brown, Ignacio Pasqualini, Nickelas Huffman, Nicolas S Piuzzi
CASE: A 24-year-old man with Klippel-Trenaunay syndrome (KTS) presented with severe knee osteoarthritis unresponsive to conservative measures. Owing to end-stage, debilitating arthritic symptoms, surgery was pursued. Careful preoperative, multidisciplinary planning/treatment included magnetic resonance imaging to characterize the venous malformations throughout the right lower extremity, preoperative sclerotherapy, sirolimus, and robotic-assisted cementless total knee arthroplasty (TKA)...
April 1, 2024: JBJS Case Connector
https://read.qxmd.com/read/38607549/giant-cerebral-cavernous-malformation-in-a-newborn-a-rare-case-report-and-review-of-literature
#27
JOURNAL ARTICLE
Ismael Moreno, Gianluca Scalia, Giuseppe Emmanuele Umana, Ciro Soriano, Isis Alcivar, Bipin Chaurasia
BACKGROUND: Cavernous malformations (CMs), also known as cavernomas or cavernous angiomas, are vascular malformations characterized by sinusoidal spaces lined by endothelial cells. Giant CMs (GCMs) are extremely rare, with limited understanding of their presentation and management. We present a case of symptomatic GCM in a newborn and review the literature on this rare entity. CASE DESCRIPTION: A 1-month-old newborn presented with focal seizures and signs of increased intracranial pressure...
April 12, 2024: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
https://read.qxmd.com/read/38607543/a-case-report-of-perihilar-cholangiocarcinoma-in-a-patient-with-situs%C3%A2-inversus-totalis
#28
JOURNAL ARTICLE
Naohiro Hirano, Masahiro Iseki, Kei Nakagawa, Masamichi Mizuma, Takashi Kamei, Ryotaro Matsumoto, Shin Miura, Kiyoshi Kume, Atsushi Masamune, Michiaki Unno
Situs inversus totalis is a rare congenital malformation in which organs are positioned in a mirror-image relationship to normal conditions. It often presents with vascular and biliary malformations. Only a few reports have pointed out the surgical difficulties in patients with situs inversus totalis, especially in those with perihilar cholangiocarcinoma. This report describes a 66-year-old male patient who underwent left hemihepatectomy (S5, 6, 7, and 8) with combined resection of the caudate lobe (S1), extrahepatic bile duct, and regional lymph nodes for perihilar cholangiocarcinoma with situs inversus totalis...
April 12, 2024: Clinical Journal of Gastroenterology
https://read.qxmd.com/read/38607271/idiopathic-intracranial-hypertension-as-the-initial-presenting-manifestation-of-systemic-lupus-erythematosus-in-a-child
#29
JOURNAL ARTICLE
Murugan Sudhakar, Anu P Kocheril, Anish S George, George I Vettiyil, Anitha Jasper, Sathish Kumar
Idiopathic intracranial hypertension (IIH) is a diagnosis of exclusion characterized by features of raised intracranial pressure (ICP) in the absence of brain parenchymal lesion, vascular malformations, hydrocephalus, or central nervous system (CNS) infection. Commonly used other terms for this entity include benign intracranial hypertension (BIH) or pseudotumor cerebri. Few case reports of systemic lupus erythematosus (SLE) presenting as IIH are available in the literature. We report a 12-year-old girl presented with chronic holocranial headache and occasional episodes of projectile vomiting for the last 6 months and then developed blurring of vision for the last month...
April 12, 2024: Lupus
https://read.qxmd.com/read/38607059/from-vessels-to-neurons-the-role-of-hypoxia-pathway-proteins-in-embryonic-neurogenesis
#30
REVIEW
Barbara K Stepien, Ben Wielockx
Embryonic neurogenesis can be defined as a period of prenatal development during which divisions of neural stem and progenitor cells give rise to neurons. In the central nervous system of most mammals, including humans, the majority of neocortical neurogenesis occurs before birth. It is a highly spatiotemporally organized process whose perturbations lead to cortical malformations and dysfunctions underlying neurological and psychiatric pathologies, and in which oxygen availability plays a critical role. In case of deprived oxygen conditions, known as hypoxia, the hypoxia-inducible factor (HIF) signaling pathway is activated, resulting in the selective expression of a group of genes that regulate homeostatic adaptations, including cell differentiation and survival, metabolism and angiogenesis...
April 3, 2024: Cells
https://read.qxmd.com/read/38604710/advances-in-intraoperative-imaging-for-vascular-neurosurgery
#31
REVIEW
Chanju Fritch, Ephraim Church, David Andrew Wilkinson
Cerebrovascular surgery has many intraoperative imaging modalities available. Modern technologies include intraoperative digital subtraction angiogram, indocyanine green (ICG) angiography, relative fluorescent measurement with ICG, and ultrasound. Each of these can be used effectively in the treatment of open aneurysm and arteriovenous malformation surgeries, in addition to arteriovenous fistula surgery, and cerebral bypass surgery.
May 2024: Neuroimaging Clinics of North America
https://read.qxmd.com/read/38602300/serum-apelin-as-a-potential-biomarker-for-infantile-hemangiomas
#32
JOURNAL ARTICLE
Qiang Chen, Yunxuan Zhang, Sili Ni, Liuqing Yang, Jiwei Li, Xingang Yuan, Meng Chen, Jing Liu, Xiaoyan Luo, Yimin Xie, Hua Wang
BACKGROUND: Infantile hemangiomas (IHs) are common benign vascular tumors in infants. Apelin, an endogenous cytokine, is implicated in the angiogenesis of neoplastic diseases. We aimed to explore the association between apelin and IHs, providing a foundation for clinical applications. METHODS: We identified differential expression of apelin in proliferative IHs compared to healthy controls (HCs) through bioinformatics analysis of publicly available databases and verified by Immunofluorescence...
April 11, 2024: Pediatric Blood & Cancer
https://read.qxmd.com/read/38601899/isolated-cavernous-venous-malformation-of-the-eyelid
#33
Khushdeep Abhaypal, Manpreet Singh, Manu Saini, Kirti Gupta, Pankaj Gupta
Cavernous hemangioma, currently known as "cavernous venous malformation," is a common, benign, non-infiltrative, slowly progressive vascular malformation of the orbit presenting in adults. We report the case of a 9-year-old girl who presented with a painless palpable mass over the right upper eyelid of 7 years' duration. A computed tomography scan of the orbits revealed a heterogeneously enhancing, well-circumscribed mass in the right upper eyelid with no orbital extension. A transcutaneous excisional biopsy with histopathology disclosed cavernous venous malformation...
2024: Digital Journal of Ophthalmology: DJO
https://read.qxmd.com/read/38598961/simulating-pdt-of-port-wine-stains-in-the-in-vivo-chicken-wattle-model-using-hemoporfin-and-radiation-at-532-nm-comparison-of-a-led-and-a-laser-source
#34
JOURNAL ARTICLE
Ziwei Guo, Weihao Zhou, Cheng Ke, Zheng Huang, Yuzhi Wang, Yingjie Zhu, Kaihua Yuan, Xiangdong Qi
Port-wine stain (PWS) birthmarks are congenital capillary malformations occurring in 0.3 %∼0.5 % of newborns. Hemoporfin-mediated vascular-acting photodynamic therapy (Hemoporfin PDT) is an emerging option for treating PWS. This in vivo study aimed to compare laser and light-emitting diodes (LED) as light source for Hemoporfin PDT. Chicken wattles were used as the animal model. Color and histopathological changes were evaluated after combining Hemoporfin with KTP laser or LED light source of 532 nm at the same doses...
April 9, 2024: Photodiagnosis and Photodynamic Therapy
https://read.qxmd.com/read/38597798/long-term-clinical-and-radiological-trajectories-of-craniocervical-vasculopathy-in-children-with-phace-syndrome
#35
JOURNAL ARTICLE
Moran Hausman-Kedem, Elysa Widjaja, Ronan J Vieira Neto, Elena Pope, Irene Lara-Corrales, Nomazulu Dlamini, Daune Macgregor, Elizabeth Pulcine, Gabrielle Deveber, Mahendranath Moharir
AIM: To describe the rates of stroke and craniocervical vasculopathy progression in children with posterior fossa malformations, hemangioma, arterial anomalies, coarctation of the aorta/cardiac defects, and eye abnormalities (PHACE) syndrome. METHOD: A single-center, retrospective natural history study of children with PHACE syndrome. Clinical and sequential neuroimaging data were reviewed to study the characteristics and progression of vasculopathy and calculate the rates of arterial ischemic stroke (AIS) and transient ischemic stroke (TIA)...
April 10, 2024: Developmental Medicine and Child Neurology
https://read.qxmd.com/read/38597545/experience-with-808-nm-diode-laser-in-the-treatment-of-47-cases-of-oral-vascular-anomalies
#36
JOURNAL ARTICLE
Fernanda Vieira Heimlich, José Alcides Almeida de Arruda, Camila de Nazaré Alves de Oliveira Kato, Leni Verônica de Oliveira Silva, Leandro Napier Souza, Marcus Vinicius Lucas Ferreira, João de Jesus Viana Pinheiro, Tarcília Aparecida Silva, Lucas Guimarães Abreu, Ricardo Alves Mesquita
Treatment of oral vascular anomalies (OVA) has focused on minimally invasive techniques rather than radical surgery. We investigated the efficacy and safety of diode laser using the photocoagulation technique in the management of OVA. Forty-seven subjects with OVA were treated with forced dehydration with induced photocoagulation (FDIP) using diode laser (808 nm/4.5 W). This series consisted mostly of male (63.8%) and non-white (63.8%) patients with a mean age of 57.4 years. Varices (91.5%), venous malformations (6...
2024: Brazilian Oral Research
https://read.qxmd.com/read/38592446/perioperative-management-of-spinal-arteriovenous-malformation-embolization-delayed-venous-thrombosis-and-implications-for-severe-back-pain
#37
JOURNAL ARTICLE
Bikei Ryu, Tatsuki Mochizuki, Shogo Shima, Shinsuke Sato, Tatsuya Inoue, Takakazu Kawamata, Yasunari Niimi
BACKGROUND AND PURPOSE: The prognosis of untreated spinal arteriovenous malformations (SAVMs) is poor. Embolization plays an important role in the management of intramedullary SAVMs. Delayed aggravation due to spinal venous thrombosis following successful embolization has been reported; however, perioperative management strategies to prevent thrombosis have not been explored. We present our single-center experience of SAVM embolization and perioperative management, including anticoagulation...
April 9, 2024: Clinical Neuroradiology
https://read.qxmd.com/read/38592015/fubuki-xf-long-sheath-guide-catheter-use-in-neuroendovascular-procedures-institutional-experience-in-60-cases
#38
JOURNAL ARTICLE
Hamzah M Saei, Samantha E Miller, Holly M Pope, Ameer E Hassan
BACKGROUND: Endovascular treatment devices require compatible guide catheters to navigate complex vessels and anatomy. The Fubuki XF Long Sheath guide catheter (Fubuki XF) was developed with a 0.090-inch internal diameter with hydrophilic coating, an atraumatic rounded tip, and enhanced trackability and support with gradual shaft transition zones. METHODS: We retrospectively analyzed a prospectively maintained database of neuroendovascular patients treated using Fubuki XF at our center (July 2022─May 2023)...
April 9, 2024: Interventional Neuroradiology
https://read.qxmd.com/read/38591305/massive-left-pulmonary-artery-aneurysm-with-a-co-existing-patent-ductus-arteriosus-in-a-five-year-old-female-child-a-case-report
#39
Javeria Khan, Muhammad Mansoor Khan, Zubair Brohi, Mahwish Mahboob, Sohail Khan Bangash
Pulmonary Artery Aneur ysm (PAA), whether congenital or acquired, is a rare diagnostic find ing com pare d to aor tic aneur ysms. There have been fe w cases where PA As were documented as a complication of untreated Patent Ductus Ar teriosus (PDA) due to long-standing Pulmonary Arterial H ypertension (PAH). However, it is quite rare for a case of PAA to be reported with co-existing PDA without PAH. This report highlights a case of a five -year-old girl who was presented with palpitations, easy fatigability, fever, c yanos is, and vomiting...
March 2024: JPMA. the Journal of the Pakistan Medical Association
https://read.qxmd.com/read/38590573/management-of-intracranial-cavernous-malformations-using-conservative-vs-surgical-and-or-radiosurgical-treatment-a-systematic-review-and-meta%C3%A2-analysis
#40
JOURNAL ARTICLE
George Fotakopoulos, Vasiliki Epameinondas Georgakopoulou, Petros Papalexis, Demetrios A Spandidos, Nikolaos Trakas, Pagona Sklapani, Kostas N Fountas
Intracranial cavernous malformations (CMs) are vascular lesions with a high bleeding rate. At present, the debate regarding their treatment is still ongoing. The present systematic review and meta-analysis aimed to evaluate the safety of surgery or radiosurgery (SRS) for the management of CMs and to determine their potential outcomes compared with conservative treatment. The present systematic review and meta-analysis investigated the relative articles involving the management of intracranial CMs, namely their natural history (conservative treatment) vs...
May 2024: Experimental and Therapeutic Medicine
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