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Laparoscopic excision of a hypervascular mass confirms hyaline vascular-type unicentric Castleman disease in a patient with diabetesSurgery for a rare mass helps a woman with diabetes

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Key Takeaway
Note that multiplanar imaging and intraoperative assessment can help avoid unnecessary pancreatic resection in suspected masses.

This case report describes the surgical management and diagnosis of a 26-year-old woman presenting with a hypervascular mass. The patient also had a history of Type 2 Diabetes Mellitus. Following laparoscopic exploration and excision of the mass, histopathological analysis confirmed a diagnosis of hyaline vascular-type unicentric Castleman disease.

Clinical follow-up for 1 year showed no residual or recurrent lesions and a stable glycemic status. The case highlights that the proximity of a mass to the pancreas does not necessarily indicate a pancreatic origin. The authors suggest that multiplanar imaging and intraoperative assessment are useful for determining the necessary extent of surgery to avoid unnecessary pancreatic resection.

Due to the nature of this report as a single case, the findings are limited by the small sample size. The results are not generalizable to a broader population, but the case provides clinical insight into the surgical management of Castleman disease in patients with comorbid Type 2 Diabetes Mellitus.

How this fits prior evidence

This case report describes a patient with Type 2 Diabetes Mellitus. While the report does not directly address the metabolic impacts of exercise or medication mentioned in prior coverage, such as the metabolic benefits of combined aerobic-resistance training or the effects of SGLT2 inhibitors and TZDs, it provides a specific clinical example of managing a localized malignancy in a patient with this underlying condition.

Imagine living with a chronic condition like Type 2 Diabetes and then discovering a mysterious growth near your pancreas. For a 26-year-old woman, this discovery led to a surgical procedure to remove a large, blood-rich mass. The surgery confirmed she had a rare condition called unicentric Castleman disease.

Doctors found that the mass was not actually part of her pancreas, even though it was located very close to it. This is a key finding because it shows that just because a growth is near an organ, it does not mean it started in that organ. This distinction is important for surgeons trying to decide how much tissue to remove during a procedure.

One year after the surgery, the woman showed no signs of the growth coming back. Her blood sugar levels also remained stable. While this was a single case, it highlights how careful imaging and checks during surgery can help doctors avoid removing healthy parts of the pancreas unnecessarily.

What this means for you:
A rare condition called Castleman disease was found in a patient with diabetes, and surgery successfully removed the mass.

Common questions

What is Castleman disease?

Castleman disease is a rare condition that can cause a growth of blood vessels. In this specific case, the patient had a type called hyaline vascular-type unicentric Castleman disease. It was found in a 26-year-old woman who also had Type 2 Diabetes.

Was the surgery successful for the patient?

Yes, the surgery was successful. One year after the removal of the mass, the patient showed no signs of the growth coming back. Additionally, her blood sugar levels remained stable following the procedure.

How does this finding help other patients?

This case shows that a mass near the pancreas is not always a problem with the pancreas itself. It suggests that using detailed imaging and checks during surgery can help doctors avoid removing healthy pancreatic tissue when it is not necessary.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedSep 2026
View Original Abstract ↓
Peripancreatic unicentric Castleman disease is rare and may mimic a primary pancreatic neoplasm because it often presents as a well-circumscribed hypervascular mass. We report a 26-year-old woman with type 2 diabetes mellitus in whom an incidentally detected upper abdominal mass was initially considered to arise from the pancreatic body. Computed tomography and magnetic resonance imaging showed a sharply marginated hypervascular lesion with diffusion restriction at the superior border of the pancreatic body, leading to a preoperative suspicion of pancreatic neuroendocrine tumor. Laparoscopic exploration revealed a well-encapsulated mass in the lesser sac closely abutting the superior surface of the pancreas. A clear dissection plane between the lesion and the pancreatic parenchyma allowed complete excision without pancreatic resection or splenectomy. Histopathological examination confirmed hyaline vascular-type unicentric Castleman disease. The postoperative course was uneventful, and no residual or recurrent lesion was detected during 1 year of follow-up; glycemic status also remained stable. This case highlights that close proximity of a hypervascular mass to the pancreas does not necessarily indicate pancreatic origin. Careful multiplanar imaging and direct intraoperative assessment of the lesion–pancreas interface may help determine the appropriate surgical extent and avoid unnecessary pancreatic resection when complete excision is technically feasible.
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