Results 121 to 130 of about 62,524 (259)

Granulocytic Sarcoma as the First Sign of Acute Leukemia in Childhood [PDF]

, 2012
Acute myeloid leukemia (AML) may rarely involve the orbit as a solid tumor termed granulocytic sarcoma. This report describes the case of a child who presented with rapidly progressive unilateral proptosis and was diagnosed as rhabdomyosarcoma.
Singh, T, Sufi, AR
core   +1 more source

HEMANGIOMAS

Annals of Surgery, 1953
J B, BROWN, M P, FRYER, F, MCDOWELL
openaire   +3 more sources

The Cervical Vertebral Bone Quality Score Is a Novel Reliable Index Reflecting the Condition of Paraspinal Muscles and Predicting Loss of Cervical Lordosis After Open‐Door Laminoplasty

Orthopaedic Surgery, Volume 17, Issue 5, Page 1406-1417, May 2025.
There is a close correlation between C‐VBQ scores and the cervical deep extensors, deep flexors, and overall paraspinal muscles relative cross‐sectional area (RCSA) and degree of fat infiltration (DFF). The C‐VBQ score is a comprehensive parameter reflecting the quality of cervical bone and paraspinal muscles.
Junhu Li, Xingxia Long, Linnan Wang, Qiujiang Li, Lei Wang, Yueming Song   +5 more
wiley   +1 more source

Corrigendum to: Efficacy and safety of sclerosants in the treatment of venous malformations: A network meta-analysis of randomized controlled trials

Chinese Journal of Plastic and Reconstructive Surgery, 2022
Wei Lu, Zhenyu Yang, Zuoliang Qi, Xiaonan Yang   +3 more
doaj   +1 more source

Clinical and radiological recurrence after childhood arterial ischemic stroke [PDF]

, 2006
Background: Data on rates and risk factors for clinical and radiological recurrence of childhood arterial ischemic stroke (AIS) might inform secondary prevention strategies.
Ganesan, V., Kirkham, F.J., Prengler, M., Wade, A.   +3 more
core  

Segmental Infantile Hemangiomas That Involve the Midline Define Risk for LUMBAR Syndrome

Pediatric Dermatology, EarlyView.
ABSTRACT A systematic review of clinical photographs from 91 patients with LUMBAR syndrome demonstrated that infantile hemangiomas in affected individuals were consistently segmental in morphology and involved the anatomic midline of the lumbosacral, sacrococcygeal, or pelvic regions. No cases were “partial segmental” or spared the midline.
D. Metry, E. Fernandez‐Faith, A. Haggstrom, K. Keppler‐Noreuil, I. J. Frieden   +4 more
wiley   +1 more source

Oral Angiolymphoid Hyperplasia With Eosinophilia Exhibiting Cutaneous‐Type Histopathologic Features: Clinical Regression Following Hormonal Withdrawal and a 50‐Year Review

Journal of Cutaneous Pathology, Volume 53, Issue 6, Page 491-501, June 2026.
Case report of a 30‐year‐old female. Asymptomatic, red‐purple hyperplastic lesion extending from teeth 21 to 25, with bleeding upon manipulation. Differential diagnosis included: inflammatory gingival hyperplasia, plasma cell gingivitis, leukemia, and Wegener's granulomatosis.
Pedro Vinícius Santos de Jesus, Louise Cristina Santos, Gilberth Tadeu Dos Santos Aciole, John Lennon Silva Cunha, Nicole Lonni, Matheus Antoni da Silva Costa, Elena Riet Correa Rivero, Rogério Gondak, Ricardo Luíz Cavalcanti de Albuquerque‐Júnior   +8 more
wiley   +1 more source

Intranodal Hemangioma: Case Report and Systematic Review

Journal of Indian Association of Pediatric Surgeons
Background: Intranodal hemangiomas are rare benign vascular tumors of the lymph nodes, often misdiagnosed as malignant lymphadenopathies due to their clinical and radiological features.
Bitesh Kumar, Kaushal Kulkarni, Dhua Anjan Kumar, Goel Prabudh, Yadav Devendra Kumar, Jain Vishesh, Agarwala Sandeep, Kaur Kavneet, Kandasamy Devasenathipathy   +8 more
doaj   +1 more source

Infarcted Melanocytic Nevus With a Hair Tourniquet

Journal of Cutaneous Pathology, EarlyView.
Aashish Batheja, Robert Bai, Joseph Gillam, Justin Haught, Mark Mochel   +4 more
wiley   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

American Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1098-1104, May 2026.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel Del Campo, Lynne M. Bird   +3 more
wiley   +1 more source