Published online Feb 6, 2022. doi: 10.12998/wjcc.v10.i4.1278
Peer-review started: August 6, 2021
First decision: November 6, 2021
Revised: November 16, 2021
Accepted: December 25, 2021
Article in press: December 25, 2021
Published online: February 6, 2022
Processing time: 171 Days and 5.1 Hours
Castleman’s disease (CD) is a lymphatic proliferative disorder of unknown cause and is rarely seen clinically. It has been divided into unicentric and multicentric types. Unicentric CD (UCD) occurs as a solitary enlarged mass and mediastinal lymph nodes are the most common site. Surgical excision has proven to be curative for UCD. Multicentric CD (MCD) appears as a systemic disease with peripheral lymphadenopathy. MCD had a poor response to surgery and mon
A 44-year-old woman presented with a pancreatic mass during routine physical examination. She had no obvious symptoms, such as fever, abdominal pain, abdominal distension, or jaundice. Ultrasound examination indicated a hypoechoic mass between the body of the pancreas, left lobe of the liver and stomach. It had a clear boundary, irregular shape, uneven echo, and no obvious blood flow signals. To clarify the diagnosis, contrast-enhanced ultrasound examination was performed, which showed a benign pancreatic lesion. Neuroendocrine or solid pseudopapillary tumor was a possible diagnosis. The patient underwent further contrast-enhanced computed tomography and contrast-enhanced magnetic resonance imaging, which were suggestive of solid pseudopapillary tumor or neuroendocrine tumor. All the examinations failed to give a definitive diagnosis, and the patient underwent surgery. The final pathological and immunohistochemical results showed that the mass was CD.
This case highlights when lymphadenopathy is encountered clinically, CD should be considered and a biopsy should be performed.
Core Tip: Castleman’s disease (CD) is a lymphoproliferative disorder of unknown cause. We present a rare case of unicentric CD. A 44-year-old woman presented with a pancreatic mass during routine physical examination. The patient had no obvious symptoms. None of the three enhanced images gave a clear diagnosis. The patient underwent surgery. The final pathological and immunohistochemical results showed that the mass was CD. This case highlights when lymphadenopathy is encountered clinically, CD should be considered and a biopsy performed. It is especially important to rule out diseases with known causes first.