Results 41 to 50 of about 3,929 (186)

Incidence of Gonadal and Extragonadal Germ Cell Tumours in Patients With Klinefelter Syndrome

open access: yesAndrology, EarlyView.
ABSTRACT Background Klinefelter's syndrome (KS; 47, XXY) is associated with an altered risk profile for malignancies compared with non‐KS males. In particular, several reports have noted a striking association between KS and extragonadal germ cell tumours (EGCTs), especially in the mediastinum, whereas the risk of testicular germ cell tumours (TGCTs ...
Aksh Tailor   +6 more
wiley   +1 more source

Predictors of Long-Term Response to Ganglion Impar Block With or Without Caudal Epidural Steroid Injection in Chronic Coccydynia: A Retrospective Study. [PDF]

open access: yesPain Res Manag
Background Ganglion impar block (GIB) is a commonly used interventional option for refractory chronic coccydynia. Caudal epidural steroid injection (CESI) targets the sacral and coccygeal roots and may theoretically augment the analgesic efficacy of GIB. Evidence comparing GIB alone with a combined GIB and CESI approach, however, remains limited.
Yavuz K   +5 more
europepmc   +2 more sources

Sacrococcygeal Pilonidal Sinus Disease: A Decade‐In‐Review of Patient‐Reported Outcome Measures

open access: yesANZ Journal of Surgery, EarlyView.
ABSTRACT Background Sacrococcygeal pilonidal sinus disease (SPD) is a chronic inflammatory condition that can significantly impact quality of life. While recurrence and surgical site infection (SSI) rates are well documented, less is known about how different surgical techniques affect patient‐reported outcome measures (PROMs).
Munyaradzi G. Nyandoro   +4 more
wiley   +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

Inguinal Dermoid Cyst Associated With Ipsilateral Undescended Testis in an Adolescent Male: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Groin swellings are the most frequent presenting clinical signs, which most frequently arise due to an inguinal hernia or lymphadenopathy. There are also rare congenital lesions, such as dermoid cysts, which can present similarly to common lesions, also leading to a diagnostic challenge.
Muhammad Hassaan Javaid   +3 more
wiley   +1 more source

Oropharyngeal teratoma: A case presentation and review of literature

open access: yesAfrican Journal of Paediatric Surgery, 2022
Teratomas are true neoplasms derived from the three germ layers. They are relatively rare tumours. They present in the sacrococcygeal region, gonads and retroperitoneum commonly.
Amina Lami Okhakhu   +1 more
doaj   +1 more source

A Clearer Picture: Using Fetal MRI to Diagnose Neck Masses and Predict Airway Compromise

open access: yesPrenatal Diagnosis, Volume 46, Issue 3, Page 339-347, March 2026.
ABSTRACT Introduction Fetal neck masses are rare but can be life‐threatening if causing airway compromise. Early and accurate diagnosis of these masses allows life‐saving interventions to be undertaken at birth in the form of the EXIT procedure. Methods A single institution case series of all patients referred for fetal MRI to a tertiary center in the ...
Louise Wilson   +2 more
wiley   +1 more source

Society for Maternal‐Fetal Medicine Consult Series #75: Evaluation and management of non‐immune hydrops fetalis

open access: yesPregnancy, Volume 2, Issue 2, March 2026.
Abstract Non‐immune hydrops fetalis (NIHF) can result from a multitude of underlying causes, such as fetal genetic diseases, congenital anomalies, infections, fetal arrhythmias, placental tumors, monochorionic twin complications, and other disorders.
Society for Maternal‐Fetal Medicine (SMFM)   +3 more
wiley   +1 more source

Sacrococcygeal chondroid chordoma: a case report and literature review

open access: yesThe Pan African Medical Journal, 2018
Chordomas are low-grade malignant tumours that arise from remnants of the notochord, usually from within the vertebral bodies It accounts for 1%-4% of malignant primary bone tumours, 50% of which are located in the sacrococcygeal region.
Fatima Zahra Farhane   +4 more
doaj   +1 more source

Aggressive fibromatosis of the leg and sacrococcygeal region: a report of two cases. [PDF]

open access: greenInt J Clin Exp Pathol, 2015
Pan F   +8 more
europepmc   +1 more source

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