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Related Experiment Videos

[Pseudolymphoma of the bladder: a case report].

H Yoshinaga, A Iguchi, Z Masaki

    Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology
    |June 1, 1989
    PubMed
    Summary

    This case study describes a rare bladder pseudolymphoma in a 63-year-old female. Chemotherapy successfully resolved the tumorous changes within six months.

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    Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.

    Clinical genetics·2014

    Area of Science:

    • Urology
    • Oncology
    • Pathology

    Background:

    • Bladder tumors can present with diverse histological features.
    • Distinguishing benign lymphoid proliferations from malignant neoplasms is crucial for appropriate management.

    Observation:

    • A 63-year-old female presented with a solid, smooth-surfaced bladder tumor (30x7 mm).
    • Biopsies revealed dense lymphocytic infiltration and lymph follicle formation, consistent with pseudolymphoma.
    • The nodular lesion was differentiated from follicular cystitis due to its size and form.

    Findings:

    • This represents a rare case of bladder pseudolymphoma, previously unreported in English literature.
    • The patient underwent a 3-week chemotherapy regimen.
    • Tumorous changes completely resolved within 6 months post-chemotherapy.

    Implications:

    • Pseudolymphoma should be considered in the differential diagnosis of bladder tumors.
    • Effective chemotherapy treatment is demonstrated for bladder pseudolymphoma.
    • This case expands the understanding of rare bladder conditions and their management.

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