Results 171 to 180 of about 726,961 (271)

Dermoid cyst associated with segmental multicystic renal dysplasia: A rare case. [PDF]

open access: yesUrol Case Rep
Laribi S   +7 more
europepmc   +1 more source

RENAL DYSPLASIA

open access: yesThe Japanese Journal of Urology, 1977
openaire   +2 more sources

Aneurysmal Bone Cyst of the Radial Diaphysis Managed by En Bloc Resection and Fibular Strut Autograft Reconstruction in a Young Adult Female: A Rare Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Aneurysmal bone cyst (ABC) of the radial diaphysis is rare and may mimic telangiectatic osteosarcoma on imaging. We report a young woman with progressively enlarging, painful forearm swelling due to ABC, treated by en bloc resection and fibular strut autograft reconstruction, achieving pain‐free union, good function and no recurrence at short ...
Abdul Hadi Khan   +6 more
wiley   +1 more source

Aggressive Hepatic AL Amyloidosis Encountering Therapeutic Frailty: Rapid Organ Reversal With Tailored Daratumumab‐Based Therapy and Low‐Dose Corticosteroids in a Patient With Steroid‐Induced Psychosis

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Hepatic AL amyloidosis can cause severe cholestasis independent of marrow tumor burden. In patients with absolute contraindications to high‐dose steroids—such as steroid‐induced psychosis—tailored daratumumab regimens with low‐dose corticosteroids can drive rapid, life‐saving organ reversal.
R. Ceccarelli   +8 more
wiley   +1 more source

Marked Hypergastrinemia and Extreme Erythrocyte Sedimentation Rate Elevation in Autoimmune Atrophic Gastritis with Severe Iron Deficiency Anemia: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Autoimmune atrophic gastritis causes loss of oxyntic glands, reduced acid secretion, compensatory hypergastrinemia, and impaired iron and vitamin B12 absorption. A 46‐year‐old woman with minimal gastrointestinal symptoms had fasting serum gastrin > 1800 ng/L, an erythrocyte sedimentation rate of 109 mm/h, hemoglobin 8.2 g/dL, and microcytosis.
Hatem Mousa Taha, Khaled Hatem Taha
wiley   +1 more source

GATA2 Deficiency Presenting With a WHIM‐Like Phenotype and Subsequent Development of Monosomy 7‐Associated Myelodysplastic Syndrome in an Adolescent Female: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT We report an 18‐year‐old female with GATA2 deficiency presenting with a WHIM‐like phenotype, including pancytopenia, monocytopenia, CD19+ B‐cell depletion, sensorineural hearing loss, and cutaneous warts. Subsequent cytogenetic evaluation revealed monosomy 7 and 7q22 deletion, with bone marrow progression to MDS.
Aziz Eghbali   +2 more
wiley   +1 more source

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. [PDF]

open access: yesLife Sci Alliance
Kim AH   +19 more
europepmc   +1 more source

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