Results 61 to 70 of about 5,736 (219)

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

open access: yesPediatric 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   +4 more
wiley   +1 more source

Radiological conference. Type I sacrococcygeal teratoma [PDF]

open access: yes, 1996
published_or_final_versio
Chan, KL, Peh, WCG
core  

Tail amputation for treatment of osteomyelitis of the first and second coccygeal vertebrae in a cow [PDF]

open access: yes, 2011
Diseases of the tail are common in cattle (3, 4). Infection or necrosis of the tail tip, injury of the coccygeal vertebrae resulting in tail paralysis (8, 12) as well as fracture or luxation of the coccygeal vertebrae(6) are some of the most common ...
Feist, M, Nuss, Karl
core   +1 more source

Teratoma of the sacrococcygeal region in children

open access: yesKazan medical journal, 2021
Among a number of congenital anomalies and deformities of the presacral area, a mixed benign tumor - teratoma - occupies one of the first places.
openaire   +2 more sources

Phenol Neurolysis in Pain and Palliative Medicine

open access: yesPain Practice, Volume 26, Issue 5, June 2026.
ABSTRACT Background Pain is a common symptom in palliative care and affects patients' quality of life considerably. Standard analgesics are sometimes insufficient and are associated with substantial side effects. Neurolysis, the targeted destruction of nerves using thermal or chemical agents, offers an additional option for managing localized pain in ...
Jeroen H. A. Creemers   +6 more
wiley   +1 more source

Imperforate hymen causing congenital hydrometrocolpos. [PDF]

open access: yes, 2013
A 3-day-old girl in good health was referred to our department for the evaluation of an abdominal mass detected at birth. Prenatal ultrasound (US) examinations had shown no anomaly.
CIGLIANO, BRUNO   +2 more
core   +1 more source

Fetus in fetu: a case report [PDF]

open access: yes, 2008
Introduction Fetus in fetu is a rare abnormality secondary to the abnormal embryogenesis in a diamniotic, monochorionic pregnancy. It is a rare pathological condition and fewer than 100 cases have been reported in the literature.
Nisreen M Khalifa   +12 more
core   +2 more sources

Tarlov Cyst with Pelvic Extension Mimicking an Adnexal Mass: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Pelvic extension of sacral Tarlov cysts can closely resemble adnexal masses on ultrasound. When cystic pelvic lesions coexist with radicular pain or sitting intolerance, MRI is mandatory prior to gynecologic surgery. Conservative treatment is preferred unless neurological deterioration occurs.
Mahsa Karbasi   +5 more
wiley   +1 more source

Demyelination and Neurological Signs in Experimental Allergic Encephalomyelitis [PDF]

open access: yes, 1987
Because of the reported absence of demyelination in some animals with neurological signs of experimental allergic encephalomyelitis (EAE), it has been suggested that these signs are not due to demyelination.
Alvord   +48 more
core   +1 more source

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome

open access: yesClinical Genetics, Volume 109, Issue 4, Page 788-795, April 2026.
We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil   +9 more
wiley   +1 more source

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