Pancreatic serous cystadenoma

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Pancreatic serous cystadenoma
Synonyms	Serous cystadenoma of the pancreas, Microcystic adenoma
Pronounce	N/A
Specialty	N/A
Symptoms	Often asymptomatic, abdominal pain, palpable mass
Complications	Rarely malignant transformation
Onset	Typically in middle-aged to elderly individuals
Duration	Chronic
Types	N/A
Causes	Unknown
Risks	Von Hippel-Lindau disease
Diagnosis	Imaging studies (e.g., CT scan, MRI), Histopathology
Differential diagnosis	Mucinous cystic neoplasm, Intraductal papillary mucinous neoplasm
Prevention	N/A
Treatment	Observation, Surgical resection if symptomatic
Medication	N/A
Prognosis	Excellent, benign behavior
Frequency	Rare
Deaths	N/A

Serous cystadenoma of the pancreatic head

Pancreatic serous cystadenoma - intermediate magnification

Pancreatic serous cystadenoma - high magnification

Pancreatic serous cystadenoma - very high magnification

Pancreatic serous cystadenoma (PSC), also known as serous cystic neoplasm of the pancreas, is a benign tumor of the pancreas. It is a type of pancreatic cyst that is typically non-cancerous and is most commonly found in the body or tail of the pancreas. PSCs account for about 1-2% of all pancreatic tumors and are more frequently diagnosed in women, particularly in the sixth and seventh decades of life.

Etiology and Pathogenesis

The exact cause of pancreatic serous cystadenoma is not well understood. These tumors are thought to originate from the centroacinar cells, which are part of the pancreatic ducts. Genetic mutations have been identified in some cases, but the significance of these mutations is still under investigation.

Clinical Presentation

Patients with pancreatic serous cystadenoma often present with non-specific symptoms or are asymptomatic. When symptoms do occur, they may include abdominal pain, nausea, and vomiting. The growth of the tumor can lead to the compression of adjacent organs, causing additional symptoms such as jaundice.

Diagnosis

Diagnosis of pancreatic serous cystadenoma typically involves a combination of imaging studies and histological examination. Computed tomography (CT) scans and magnetic resonance imaging (MRI) are commonly used to visualize the cystic nature of the tumor and its location within the pancreas. Endoscopic ultrasound (EUS) with fine-needle aspiration (FNA) may be employed to obtain tissue samples for histological analysis.

Treatment

The treatment approach for pancreatic serous cystadenoma depends on the size of the tumor, its location, and the presence of symptoms. Asymptomatic small tumors may be managed with regular monitoring and follow-up imaging studies. Surgical resection is recommended for symptomatic tumors, tumors that are increasing in size, or when malignancy cannot be ruled out. The most common surgical procedures are the distal pancreatectomy and enucleation.

Prognosis

The prognosis for patients with pancreatic serous cystadenoma is generally excellent, as these tumors are benign and have a low potential for malignancy. Surgical removal of the tumor is usually curative, and recurrence is rare.

Epidemiology

Pancreatic serous cystadenomas are more common in women than in men and are typically diagnosed in individuals over the age of 60. The incidence of these tumors is relatively low, making up about 1-2% of all pancreatic neoplasms.

Images

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  Pancreatic serous cystadenoma

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  Pancreatic serous cystic tumor

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  Relative incidence of pancreatic neoplasms

See Also

• Pancreatic cancer
• Pancreatic cyst
• Pancreatic neoplasm

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