Back to Authors

Ghosh, Amit Kumar

https://orcid.org/0000-0002-8894-4078

Mayo Clinic

Mayo Clinic

Citations 2

Spontaneous Tumor Lysis Syndrome in the Setting of B-Cell Lymphoma
Figanbaum, Travis, Ghosh, Amit Kumar , Caples, Sean M., Opyrchal, Mateusz , Figanbaum, Travis L., Rajkumar, S. Vincent

Case Reports in Medicine | March 11, 2010 | Volume: 2010 | Issue: No issue available | Pages: 1-3

10.1155/2010/610969 Get It

Tumor lysis syndrome (TLS) presenting in absence of chemotherapy is a rare occurrence. One of the true oncological emergencies, it can lead to significant morbidity and mortality. TLS is a phenomena usually associated with tumor cell death after treatment. The etiology of the spontaneous TLS is not well understood, which complicates the diagnosis. TLS is well known to oncologists but physicians outside of this specialty have little or no experience with this condition. Early recognition and treatment are the keys to limiting the sequela of the condition. Spontaneous tumor lysis syndrome is rare but presents added risks to the patient because of the potential for delayed diagnosis and no benefit of pretreatment. Diagnosis may be further delayed because this may be the first symptom of underlying malignancy. Therefore, it is imperative that all clinicians are familiar with the syndrome to assure timely recognition.
Radiation arteritis following treatment for Wilms’ tumor: an unusual case of weight loss
Ghosh, Amit Kumar , Lundstrom, Carl E, Edwards, William D.

Vascular Medicine | October 11, 2002 | Volume: 7 | Issue: 1 | Pages: 19-23

10.1191/1358863x02vm408cr Get It

Wilms’ tumor is the most common pediatric primary renal cancer and is highly responsive to surgery and chemotherapy. The role of radiotherapy has evolved in the last three decades from the use of stepwise incremental doses in all patients to the current concept of added radiotherapy in advanced cases or in those with unfavorable pathology. To the authors’ knowledge, this is the first case of a young woman with prior history of Wilms’ tumor and significant weight loss due to radiation arteritis involving the abdominal vasculature. A 31-year-old woman presented with a history of weight loss and severe malnutrition. An angiogram revealed that the aorta was occluded below the renal artery. The celiac artery and the superior mesenteric artery were occluded at the origin, and large intercostal collaterals reconstituted the pelvic circulation. She was initially treated with total parenteral nutrition (TPN) and underwent an infrarenal aortic bypass surgery. Histopathology of the aorta revealed intimal fibrocalcific thickening and changes consistent with radiation-induced arteritis. Later, she was readmitted with progressive hepatic insufficiency. Despite intensive medical therapy, she died of multi-organ failure.