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Characterization of Pancreatic Serous Cystadenoma on Dual-Phase Multidetector CT

 

 

Characterization of Pancreatic Serous Cystadenoma on Dual-Phase Multidetector CT

LC Chu, MD

Johns Hopkins University

 

Introduction

  • Pancreatic serous cystic neoplasms account for approximately 20% of primary cystic pancreatic neoplasms1
  • Most serous cystic neoplasms are benign and represent serous cystadenomas (SCAs)1
  • Classically, serous cystadenomas have been described as multilocular well-circumscribed masses that contain a central stellate scar and calcifications2
  • However, serous cystadenomas have a wide spectrum of CT appearance ranging from an unilocular cystic lesion to a solid hypervascular mass3

 

Introduction

  • The CT appearance of SCAs may overlap with potentially malignant cystic neoplasms such as mucinous cystic neoplasms and intraductal mucinous neoplasms (IPMNs)4
  • Due to rarity of SCAs and variable CT appearance, accuracy of preoperative CT diagnosis has been reported to be as low as 23.3%5
  • The predictive value of CT for diagnosis of SCAs improved with increasing number of detectors5
  • Therefore, further characterization of CT features on dual-phase multidetector may improve diagnostic accuracy of SCAs

 

Purpose

  • To characterize morphologic features and CT attenuation of pancreatic serous cystadenomas on dual-phase multidetector CT
  • To determine CT features which may be useful in differentiating serous cystadenomas from other pancreatic lesions
  • To review the management implications

 

Methods

  • Institutional review board approved retrospective study
  • From January 2003 to December 2010, 68 patients with surgically resected and pathologically confirmed pancreatic serous cystadenomas were identified from the pathology database
  • 68 patients had preoperative dual-phase multidetector CT examinations 40 female, 28 male, mean age 58
  • CT examinations were performed on a 16-slice, 64-slice, or dual source multidetector CT

 

MDCT Protocol

MDCT Protocol

 

Qualitative Assessment

All CT examinations were retrospectively reviewed to determine location, size, and morphologic features of the serous cystadenomas:
  • +/- Septations
  • +/- Calcifications
  • +/- Peripheral rim enhancement
  • +/- Main pancreatic duct (MPD) dilatation
  • +/- Common bile duct (CBD) dilatation
  • +/- Vascular invasion
  • +/- Suspicious liver mass
  • +/- Mesenteric lymphadenopathy

 

Quantitative Assessment

Quantitative CT attenuation measurements using a 1cm2 ROI:
  • Arterial phase:
    • Region of highest attenuation within the SCA
    • Region of lowest attenuation within the SCA
    • Background pancreas
  • Portal venous phase:
    • Corresponding highest and lowest attenuation regions
    • Background pancreas
Quantitative Assessment

 

Results

  • 70 serous cystadenomas were identified in 68 patients
  • Mean maximal axial dimension = 4.5 cm
    • Range: 1.0 cm to 12.2 cm
  • Location:
    • Head (29%)
    • Neck (6%)
    • Body (27%)
    • Tail (39%)

 

External Margins

External Margins

The majority of SCAs (70%) had lobulated external margins

 

Internal Septations

Internal Septations

Most of SCAs (83%) had multiple internal septations

 

Internal Calcifications

Internal Calcifications

36% of lesions contained internal calcifications
  • ~ Half of the calcifications were located centrally
  • Less than half of the calcifications were located peripherally

 

Peripheral Rim Enhancement

Peripheral Rim Enhancement

Peripheral rim enhancement was present in less than one-third of lesions on both arterial phase and portal venous phase

 

MPD and CBD Dilatation

MPD and CBD Dilatation

Dilatation of the main pancreatic duct and common bile duct were uncommon

 

Vascular Involvement

Vascular Involvement

  • Vascular displacement due to mass effect was uncommon
  • Vascular occlusion was rare

 

Additional Features

  • Atrophy or fatty replacement of background pancreas (11%)
  • No suspicious liver lesion
  • No mesenteric lymphadenopathy

 

CT Attenuation

CT Attenuation

 

Subgroup Analysis

  • Pancreatic SCAs were subdivided based on CT attenuation and morphologic features:
    • Oligocystic (9%)
      • < 6 cysts, each cyst > 2 cm
    • Polycystic (37%)
      • > 6 cysts, each cyst < 2 cm
    • Cystic and solid (34%)
      • Contains both soft tissue component and cystic component
    • Solid (20%)
      • Soft tissue attenuation without identifiable cysts

 

Subgroup Analysis

Subgroup Analysis

 

CT Attenuation of Subgroups – Arterial Phase

CT Attenuation of Subgroups – Arterial Phase

*95% confidence interval for mean attenuation

 

CT Attenuation of Subgroups – Portal Venous Phase

CT Attenuation of Subgroups – Portal Venous Phase

*95% confidence interval for mean attenuation

 

Discussion

Discussion
  • “Classic” serous cystadenoma has been described as a cystic lesion with:2
    • Multiple thin non-enhancing septations
    • Central calcifications
    • Absence of main pancreatic duct dilatation
    • Absence of vascular involvement
  • 20% of the cases fulfill this “classic” description

 

“Classic” Serous Cystadenoma – By Size

  • “Classic” SCAs were generally larger in size: (p = 0.005)
    • Mean diameter of “classic” lesion = 6.3 cm
    • Mean diameter of “non-classic” lesion = 4.0 cm
  • Higher percentage of larger SCAs demonstrated “classic” morphology
    • Lesion < 3cm: 7% with “classic” morphology
    • Lesion > 3cm: 29% with “classic” morphology

 

“Classic” Serous Cystadenoma – By Attenuation

“Classic” Serous Cystadenoma – By Attenuation

“Classic” SCAs demonstrated lower attenuation compared to “non-classic” SCAs

 

Correlation between CT Attenuation and Pathologic Classification

  • Traditional classification of SCAs was based on imaging and gross pathologic features:3,6
    • Microcystic (70%)
    • Honeycomb (20%)
    • Oligocystic (<10%)
  • Classification of SCAs based on CT attenuation and morphologic features:
    • Polycystic (37%)
    • Cystic and solid (34%)
    • Solid (20%)
    • Oligocystic (9%)

 

Correlation between CT Attenuation and Pathologic Classification

  • The polycystic pattern and cystic and solid pattern fit into the microcystic category and represented the most common CT appearance of serous cystadenomas
  • Most of the solid cystadenomas fit into the honeycomb category, in which the individual cysts were too small to be resolved on CT
  • One of the solid cystadenomas was a rare solid variant of serous cystadenoma, which did not contain any cystic spaces on histopathology

 

Correlation between CT Attenuation and Pathologic Classification

Correlation between CT Attenuation and Pathologic Classification

 

CT Attenuation As Compared to Other Cystic Pancreatic Lesions

CT Attenuation As Compared to Other Cystic Pancreatic Lesions

Chalian et al. (2011) reported mean CT attenuation values of unilocular cystic pancreatic lesions during the pancreatic parenchymal phase:7
  • Pseudocyst 18.9 HU ± 3.8
  • Mucinous cystic neoplasms 13 HU ± 2.5
  • IPMNs 11.4 HU ± 2.7

 

Differentiating Oligocystic and Polycystic SCAs from Other Cystic Pancreatic Lesions

  • DDX: Mucinous cystic neoplasm, pseudocyst, IPMN
  • External Contour:
    • External lobulations has been reported as a specific feature for SCAs4,8
      • 72% of oligocystic and polycystic SCAs demonstrated external lobulations
    • Mucinous cystic neoplasm: Smooth contour
    • Pseudocyst: Smooth contour
    • IPMN: Pleomorphic or clubbed fingerlike cystic shape
  • Fibrous Central Scar ± Calcifications:
    • Highly specific and virtually path gnomonic for SCA6
Differentiating Oligocystic and Polycystic SCAs from Other Cystic Pancreatic Lesions

 

Differentiating Oligocystic and Polycystic SCAs from Other Cystic Pancreatic Lesions

  • Pancreatic Duct:
    • SCA: No communication with pancreatic duct
    • IPMN: Communication with pancreatic duct
  • CT Attenuation Values:
    • Similar to reported values for pseudocyst, mucinous cystic neoplasms, and IPMNs
  • Clinical Information:
    • SCA: No history of pancreatitis
    • Pseudocyst: History of pancreatitis

 

CT Attenuation As Compared to Other Solid Pancreatic Lesions

CT Attenuation As Compared to Other Solid Pancreatic Lesions

  • Yoon et al. (2011) reported mean CT attenuation values for pancreatic adenocarcinoma:9
    • Pancreatic parenchymal phase – 109.4 HU
    • Hepatic venous phase – 96.0 HU
  • Liu et al. (2009) reported mean CT attenuation values for insulinomas:10
    • Arterial phase – 114.48 ± 27.30 HU
    • Portal venous phase – 112.19 ± 19.52 HU

 

Differentiating Solid SCAs from Other Solid Pancreatic Lesions

  • DDX: Adenocarcinoma, islet cell tumor, solid pseudopapillary tumor
  • Pancreatic Duct and Common Bile Duct Dilatation:
    • SCA: Uncommon
    • Adenocarcinoma: Common
  • Vascular Involvement:
    • SCA: May compress adjacent vessels due to mass effect, vascular occlusion rare
    • Adenocarcinoma: Vascular involvement frequently seen, important determinant in resectability

 

Differentiating Solid SCAs from Other Solid Pancreatic Lesions

  • Liver Metastasis and Mesenteric Lymphadenopathy:
    • Absent in SCAs
    • May be seen in serous cystadenocarcinoma (extremely rare)
    • Presence suggestive of adenocarcinoma or islet cell tumor
  • CT Attenuation Values:
    • May overlap with adenocarcinoma and islet cell tumor
  • Clinical Information:
    • Older age group than solid pseudopapillary tumor
    • Absence of symptoms associated with functioning islet cell tumor

 

Management

  • Important to differentiate serous cystadenoma from other malignant or premalignant lesions
  • Management of SCAs depend on patients’ age and comorbidities, tumor size and location, presence or absence of symptoms, local practice patterns, and surgeon preferences5
  • If diagnosis of SCA can be made based on imaging and laboratory findings, surgical resection is usually reserved for:11
    • Symptomatic patients
    • > 4cm in size regardless of symptoms

 

Management

  • However, many SCAs do not demonstrate “classic” imaging characteristics and remain indeterminate
  • ACR Guidelines for management of pancreatic cystic lesions17:
    • < 2cm: Single follow-up in 1 year, no further follow-up if asymptomatic
    • 2 to 3 cm:
      • Mucinous: Follow-up every 6 months
      • Uncharacterized: Follow-up yearly
      • Serous cystadenoma: Follow-up every 2 years
    • > 3cm: Consider surgery
    • Endoscopic ultrasound and cyst aspiration may be useful adjuncts

 

Strengths of the Current Study

  • All cases of serous cystadenomas were surgically resected and pathologically proven
  • All preoperative dual-phase multidetector CTs were performed with consistent technique, which allowed for:
    • Qualitative morphologic assessment
    • Quantitative CT attenuation measurements

 

Weaknesses of the Current Study

  • This retrospective surgical series may contain a higher proportion of atypical cases
    • Typical cases based on CT morphology may not be referred to surgery and were excluded
  • CT acquisition and ROI measurement techniques were not the same as previous studies
    • We elected to measure regions with the highest and lowest attenuation due to the variability of attenuation within the same lesion
    • Limited comparison of CT attenuation among various pancreatic lesions

 

Conclusions

  • “Classic” morphology of pancreatic serous cystadenoma was uncommon and only found in 20% of cases
  • Most common CT appearance of serous cystadenoma was a polycystic or mixed cystic and solid mass
  • Wide spectrum of CT appearances ranging from unilocular cyst to hypervascular solid mass

 

Conclusions

  • Significant overlap in CT attenuation among serous cystadenoma and other cystic and solid pancreatic lesions
  • Presence of external lobulations useful in differentiating serous cystadenomas from other cystic pancreatic lesions
  • Absence of aggressive features useful in differentiating serous cystadenomas from solid malignant pancreatic lesions

 

References

  1. Basturk O, et al. Arch Pathol Lab Med 2009;133:423-438
  2. Curry CA, et al. AJR 2000;175:99-103
  3. Kim HJ, et al. AJR 2008; 190:406-412
  4. Kim SY, et al. AJR 2006; 187:1192-1198
  5. Khashab MA, et al. Am J Gastroenterol 2011; 106:1521-1526
  6. Sahani DV, et al. Radiographics 2005; 25:1471-1484
  7. Chalian H, et al. JOP 2011; 12:384-388
  8. Cohen-Scali F, et al. Radiology 2003; 228:727-733
  9. Yoon SH, et al. Radiology 2011; 259-442-452
  10. Liu Y, et al. Radiol Med 2009; 114:1232-1238
  11. Berland LL, et al. J Am Coll Radiol 2010; 7:754-773

Acknowledgements

  • LC Chu, MD
  • AD Singhi, MD PhD
  • RH Hruban, MD
  • EK Fishman, MD

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