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Published on: June 9, 2021
Rhabdomyolysis caused by peripheral T-cell lymphoma in skeletal muscle
Koichi Sasaki1, Masaya Yamato, Keiko Yasuda
1Department of Nephrology, Osaka Kosei Nenkin Hospital, Osaka, Japan.
Insights
Peripheral T-cell lymphoma (PTCL) can cause rhabdomyolysis, a rare condition leading to muscle breakdown and acute kidney injury. Early diagnosis and treatment of PTCL are crucial for managing this complication.
Area of Science:
- Oncology
- Nephrology
- Pathology
Background:
- Peripheral T-cell lymphoma (PTCL) is a heterogeneous group of aggressive non-Hodgkin lymphomas.
- Rhabdomyolysis, the breakdown of skeletal muscle tissue, can lead to acute kidney injury.
- The association between PTCL and rhabdomyolysis is rare and not well-documented.
Observation:
- A 62-year-old male presented with sudden muscle weakness, elevated creatinine phosphokinase (62,640 IU/L), and acute kidney injury (serum creatinine 5.0 mg/dL).
- Imaging revealed tumorous swelling in the psoas major and obturator internus muscles.
- The patient subsequently developed fever and hemophagocytic syndrome, with markedly elevated ferritin levels (104,707.0 ng/mL).
Findings:
- Inguinal lymph node biopsy confirmed the diagnosis of PTCL.
- The patient was diagnosed with rhabdomyolysis secondary to PTCL.
- Treatment with hydration, hemodiafiltration, and methylprednisolone pulse therapy led to significant improvement in renal function and tumor reduction.
Implications:
- This case highlights that PTCL should be considered in the differential diagnosis of unexplained rhabdomyolysis, especially in the absence of common causes like trauma or drug toxicity.
- Prompt recognition and management of PTCL-induced rhabdomyolysis can improve patient outcomes and prevent irreversible kidney damage.
- Further research is warranted to understand the underlying mechanisms linking PTCL and skeletal muscle injury.
Abstract:
We report a rare case of rhabdomyolysis caused by peripheral T-cell lymphoma (PTCL) in skeletal muscle. A 62-year-old man was admitted with complaints of sudden muscle weakness. Laboratory abnormalities were identified including markedly elevated creatinine-phosphokinase, peaking at 62,640 IU/L and serum creatinine (Cr) at 5.0 mg/dL. Computed tomography scans revealed tumorous swelling of the right psoas major muscle and the obturator internus muscles. Consequently, he was diagnosed with acute renal failure caused by rhabdomyolysis and was treated with hydration and continuous hemodiafiltration, which resulted in significant improvement in renal function (Cr 1.79 mg/dL). However, the cause of the rhabdomyolysis remained unclear, and he suddenly developed a remittent fever and suffered from hemophagocytic syndrome. Serum ferritin level dramatically increased to 104,707.0 ng/mL and creatinine level to 4.09 mg/dL. We performed a biopsy of inguinal lymph nodes, leading to a diagnosis of PTCL. Finally, he was diagnosed with rhabdomyolysis caused by PTCL. Methylprednisolone pulse therapy markedly improved his general condition and renal function (Cr 1.48 mg/dL), and computed tomography scans revealed that tumorous swelling was greatly diminished. Except when the cause of rhabdomyolysis is readily apparent, such as in cases of trauma, drug and thrombophlebitis, one should consider that rhabdomyolysis may be a sequel of lymphoma.
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