Evidence map›Paper›PMID 42466215›Full record

ArticleEuropean journal of case reports in internal medicine2026

Isolated Bilateral Nephromegaly as the Initial Presentation of Acute Lymphoblastic Leukaemia: A Rare Case and Review of the Literature.

Rawan Hamdan, Mais Musleh, Mahmoud Alhamadeh Alswij, Yara Ibraheem, Miriam Laflouf, Abdulhalim Mohamed Alyousef

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Article in European journal of case reports in internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Rawan HamdanDepartment of Hematology, Al-Mouwasat University Hospital, Damascus, Syria.
Mais MuslehDepartment of Hematology, Al-Mouwasat University Hospital, Damascus, Syria.
Mahmoud Alhamadeh AlswijDepartment of Internal Medicine, Hematology Department, Al Mouwasat University Hospital, Damascus, Syria.
Yara IbraheemDepartment of Nephrology, Al-Mouwasat University Hospital, Damascus, Syria.
Miriam LafloufDepartment of Hematology, Al-Mouwasat University Hospital, Damascus, Syria.
Abdulhalim Mohamed AlyousefDepartment of Hematology, National University Hospital, Damascus, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Acute lymphoblastic leukaemia (ALL) is an aggressive hematologic malignancy, with T-cell ALL (T-ALL) accounting for approximately 25% of adult cases. Renal infiltration is recognized but rarely presents as isolated bilateral nephromegaly with acute kidney injury (AKI) in adults. Case description: A 32-year-old previously healthy man presented with progressive bilateral flank pain, abdominal heaviness, fatigue, intermittent fever, night sweats, and unintentional weight loss. Physical examination revealed large bilateral flank masses without peripheral lymphadenopathy. Laboratory tests initially showed normal blood counts but significant renal impairment (creatinine 3.5 mg/dl, urea 82 mg/dl). Imaging demonstrated massive bilateral kidney enlargement (~20 × 20 cm). Percutaneous renal biopsy revealed diffuse infiltration by medium-sized lymphoblasts expressing CD3 and TdT, confirming T-ALL. Within 1-week, hematologic abnormalities developed, including leucocytosis, anaemia, and thrombocytopenia, alongside worsening renal function and tumour lysis syndrome, necessitating dialysis and allopurinol therapy. The patient was started on a pre-phase corticosteroid regimen followed by intensive hyper-CVAD (hyperfractionated cyclophosphamide, vincristine, doxorubicin [Adriamycin], and dexamethasone) induction chemotherapy. Initial radiologic improvement occurred; however, the clinical course was complicated by neutropenic sepsis, ultimately resulting in death. Conclusion: This case highlights a rare adult presentation of T-ALL in which renal involvement preceded hematologic abnormalities. Clinicians should consider hematologic malignancy in adults presenting with unexplained bilateral nephromegaly and AKI, even if initial blood counts are normal. Early recognition and timely intervention are critical to improve renal and overall outcomes. LEARNING POINTS: Renal infiltration is recognized but rarely presents as isolated bilateral nephromegaly with acute kidney injury (AKI) in adults.This report underscores the importance of considering underlying hematologic malignancy in adults presenting with unexplained bilateral nephromegaly and AKI, even when initial hematologic investigations are normal.

Indexed as

acute lymphoblastic leukaemiaKidney infiltration

Identifiers

PMID42466215
PMCPMC13374687

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