Literature DB >> 26943381

Mucinous cystic neoplasm of the pancreas activated during pregnancy.

Keisuke Kosumi1, Hiroshi Takamori2, Daisuke Hashimoto3, Hiroshi Tanaka4, Shinya Abe5, Osamu Nakahara6, Kei Horino7, Hideo Baba8.   

Abstract

The characteristic histological feature of pancreatic mucinous cystic neoplasm (MCN) is ovarian-like stroma (OS) underlying the epithelium and existence of estrogen receptors and progesterone receptors in the nucleus of OS. We experienced a case of pancreatic MCN which was activated during pregnancy and confirmed the existence of estrogen receptors and progesterone receptors. In cases with potential factors for malignancy, surgical resection of MCN may be needed during pregnancy. On the other hand, in cases without these, as female sex hormones may have an influence on the behavior of pancreatic MCN during pregnancy, the timing of surgery should be decided on a case-by-case basis, taking into consideration the status of the malignancy, the stage of the pregnancy, and the condition of the mother and fetus.

Entities:  

Keywords:  Activation; Mucinous cystic neoplasm; Pancreas; Pregnancy

Year:  2015        PMID: 26943381      PMCID: PMC4747942          DOI: 10.1186/s40792-014-0012-2

Source DB:  PubMed          Journal:  Surg Case Rep        ISSN: 2198-7793


Background

A mucinous cystic neoplasm (MCN) is relatively rare, accounting for about 8% of resected cystic lesions of the pancreas [1]. And the characteristic histological feature is ovarian-like stroma (OS) underlying the epithelium [2]. As with an ovarian MCN, estrogen receptors (ER) and progesterone receptors (PgR) are expressed in OS of pancreatic MCN [3], indicating that female sex hormones may have an influence on the behavior of pancreatic MCN, especially during pregnancy. We experienced a patient with pancreatic MCN which was activated during the pregnancy. Herein, we introduce the case, together with a literature review of MCN during pregnancy.

Case presentation

A 33-year-old woman who was 4 months pregnant complained of left back pain. Abdominal ultrasound revealed a 60-mm cystic mass in the body and tail of the pancreas without a mural nodule or thickening of the wall (Figure 1a). The serum cancer antigen (CA) 19-9 level was elevated, at 92 U/mL (normal level is <37 U/mL), and then rapidly rose to 2,157 U/mL just before delivery.
Figure 1

Imaging studies. (a) A 60-mm cystic mass was detected in the body and tail of the pancreas without a mural nodule or thickening of the wall by abdominal ultrasound (during the fourth month of gestation). (b) Magnetic resonance imaging (MRI) showed a 76 × 69-mm cystic tumor (arrow), in which the contents were hyperintense in T2-weighted imaging. There were septa in the tumor, and one part of it was thickened and enhanced. (c) Fluorodeoxyglucose positron emission tomography-computed tomography (FDG-PET/CT) showed high uptake (arrow) in part of the cystic tumor (SUVmax 3.03).

Imaging studies. (a) A 60-mm cystic mass was detected in the body and tail of the pancreas without a mural nodule or thickening of the wall by abdominal ultrasound (during the fourth month of gestation). (b) Magnetic resonance imaging (MRI) showed a 76 × 69-mm cystic tumor (arrow), in which the contents were hyperintense in T2-weighted imaging. There were septa in the tumor, and one part of it was thickened and enhanced. (c) Fluorodeoxyglucose positron emission tomography-computed tomography (FDG-PET/CT) showed high uptake (arrow) in part of the cystic tumor (SUVmax 3.03). The patient's antenatal course was uneventful, and the delivery was normal. After delivery, magnetic resonance imaging revealed that the cystic tumor was 76 mm in diameter, with a thickening septum seen on T2-weighted imaging (Figure 1b). In addition, fluorodeoxyglucose positron emission tomography-computed tomography (FDG-PET/CT) showed an abnormally high uptake in part of the cystic tumor (Figure 1c). As FDG-PET/CT imaging indicated that malignancy could not be excluded, the patient underwent distal pancreatectomy on the 14th day after delivery (Figure 2a,b). Microscopically, the cyst wall was lined with benign mucinous columnar epithelium underlying OS (Figure 3a). In addition, immunohistochemical analysis showed that both ER and PgR were partially positive in the nucleus of OS (Figure 3b,c).
Figure 2

Intraoperative findings and macroscopic observations. (a) A smooth cystic tumor occupied the body and tail of pancreas (arrowheads indicating the tumor). Distal pancreatectomy was performed. (b) The cut surface of the tumor showing a large cyst without solid components.

Figure 3

Analysis of pancreatic mucinous cystic adenoma by immunohistochemistry. (a) The cyst wall was lined with benign mucinous columnar epithelium underlying OS (Hematoxylin and eosin, ×100). (b) Immunohistochemical studies showed partial positive staining for estrogen receptors in the nucleus of ovarian-type stroma (×100). (c) Immunohistochemical studies showed partial positive staining for progesterone receptors in the nucleus of ovarian-type stroma (×100).

Intraoperative findings and macroscopic observations. (a) A smooth cystic tumor occupied the body and tail of pancreas (arrowheads indicating the tumor). Distal pancreatectomy was performed. (b) The cut surface of the tumor showing a large cyst without solid components. Analysis of pancreatic mucinous cystic adenoma by immunohistochemistry. (a) The cyst wall was lined with benign mucinous columnar epithelium underlying OS (Hematoxylin and eosin, ×100). (b) Immunohistochemical studies showed partial positive staining for estrogen receptors in the nucleus of ovarian-type stroma (×100). (c) Immunohistochemical studies showed partial positive staining for progesterone receptors in the nucleus of ovarian-type stroma (×100). All pancreatic MCNs should be resected because they are considered as having malignant potential [4]. As increase in tumor size, mural nodules, and eggshell calcification predict malignant MCN [5], the ideal strategy is to remove the MCN surgically before these predictors develop. However, it is difficult to determine the best timing for surgery when pancreatic MCN is detected during pregnancy. There are several points of view. First, an accurate diagnosis of malignancy is difficult, especially for borderline cases. Second, it is necessary to consider the effects of surgery on the mother and the fetus. We analyzed the clinical characteristics of MCNs detected during pregnancy according to data extracted from our case and previous reports [6-24], as well as our own experience (Table 1). In the reports reviewed, 12 patients underwent surgery during pregnancy, and neither miscarriage nor operation-related death occurred in any of the patients. Eight patients underwent operation after delivery. Regarding histopathological diagnosis, 14 patients were diagnosed with benign MCN, and 6 patients, 3 patients underwent operation during pregnancy and 3 patients after delivery, were diagnosed with adenocarcinoma. Among the six patients with adenocarcinoma, at least four patients were alive 1 year after resection.
Table 1

Literatures review of clinical characteristics of mucinous cystic neoplasm during pregnancy

Author [reference number] Age Maximum diameter of tumor (cm) Diameter of tumor growth during pregnancy (mm) CA19-9 (U/mL) Timing of operation Histological diagnosis ER/PgR Prognosis (years)
Smithers [6]3310NANADuring pregnancyAdenocarcinomaNANA
Baiocchi [7]29NANANAAfter deliveryAdenocarcinomaNAAlive (2)
Olsen [8]2550NADuring pregnancyBenignNA
Ganepola [9]371265NADuring pregnancyBenign+/+
Kato [10]3322+NADuring pregnancyBenign+/+
Matsunaga [11]2820+NADuring pregnancyAdenocarcinoma−/+NA
Fernandez [12]2615NANADuring pregnancyBenignNA
Herring [13]342080NADuring pregnancyAdenocarcinoma+/+Alive (NA)
Ozden [14]3215NANAAfter delivery (emergency cesarean)Adenocarcinoma−/−Alive (1)
Ishikawa [15]331860NAAfter deliveryBenign−/−
Ikuta [16]3018NANormalAfter delivery (abortion)Benign+/+
Hakamada [17]381440NADuring pregnancyBenignNA/+
Wiseman [18]3215NANADuring pregnancyBenign+/+
Brown [19]3810NANADuring pregnancyBenignNA
Shirakawa [20]34190ElevatedAfter deliveryBenign+/+
Asciutti [21]31865214After deliveryBenignNA
Nagamura [22]3211NA4,750After delivery (emergency cesarean)Adenocarcinoma−/+Alive (3)
Boyd CA [23]2117.20NADuring pregnancyBenignNA
Tsuda [24]28141010During pregnancyBenign+/+
Present case337.6162,157After deliveryBenign+/+

CA19-9, cancer antigen 19–9; ER, estrogen receptor; NA, not available; PgR, progesterone receptor.

Literatures review of clinical characteristics of mucinous cystic neoplasm during pregnancy CA19-9, cancer antigen 19–9; ER, estrogen receptor; NA, not available; PgR, progesterone receptor. Importantly, in our case, we also confirmed the existence of ER and PgR. In addition, we confirmed rapid growth of MCN during pregnancy in nine patients, and at least seven patients of them showed positive staining for ER or PgR. Interestingly, Tanaka et al. reported a case of MCN developing during continuous hormone replacement therapy after hysterectomy. These findings suggested that the existence of ER and PgR might contribute to the activation of MCN during pregnancy. Although the cutoff value of size and the mural nodule diameter for predicting malignancy has not been determined, it was generally reported that factors for predicting malignant MCN were large size and the existence of mural nodes [25]. In our case, we detected not only the two signs of malignant MCN but also an elevated CA19-9 level from 92 to 2,157 U/mL. A CA19-9 concentration >37 U/mL had a positive predictive value of 95.7% for potentially malignant lesions, but only showed a sensitivity of 35.8% [26]. In Table 1, five of the six patients showed the elevation of serum CA19-9 level, and the serum CA19-9 level of the patient with adenocarcinoma was remarkably higher. However, we could not find any relationships between the expression of hormone receptors and CA19-9 level, so further studies are necessary to validate the relationship between tumor markers and clinicopathological features including malignancy and hormone receptors. In cases with potential factors for malignancy like large size and thickening septum, surgical resection of MCN may be needed. On the other hand, no findings of malignancy may enable the extension of surgical resection until delivery. In evaluating the possibility of malignant status of a MCN, consideration must be given to the stage of pregnancy and the condition of the mother and the fetus, and the timing of surgery should be decided on a case-by-case basis. Moreover, in view of the existence of ER and PgR, careful observation is necessary concerning the growth and progression of MCN.

Conclusions

In cases with potential factors for malignancy, surgical resection of MCN may be needed during pregnancy. On the other hand, in cases without these, as female sex hormones may have an influence on the behavior of pancreatic MCN during pregnancy, the timing of surgery should be decided on a case-by-case basis, taking into consideration the status of the malignancy, the stage of the pregnancy, and the condition of the mother and fetus.

Consent

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
  24 in total

Review 1.  Pancreatic neoplasms in pregnancy: diagnosis, complications, and management.

Authors:  Casey A Boyd; Jaime Benarroch-Gampel; Gokhan Kilic; Edward J Kruse; Sharon M Weber; Taylor S Riall
Journal:  J Gastrointest Surg       Date:  2011-12-09       Impact factor: 3.452

Review 2.  [Mucinous cystic neoplasm of the pancreas associated with pregnancy: report of two cases].

Authors:  Sachiyo Shirakawa; Ippei Matsumoto; Syunji Nakayama; Hideyo Mukubo; Hirochika Toyama; Makoto Shinzeki; Takumi Fukumoto; Tetsuo Ajiki; Yonson Ku
Journal:  Nihon Shokakibyo Gakkai Zasshi       Date:  2010-11

3.  Huge mucinous cystadenoma of the pancreas developing during pregnancy: a case report.

Authors:  Masato Kato; Keiichi Kubota; Junji Kita; Mitsugi Shimoda; Kyu Rokkaku; Noriyuki Inaba; Ichio Fukasawa; Kouichi Honma
Journal:  Pancreas       Date:  2005-03       Impact factor: 3.327

4.  Cystadenocarcinoma of the pancreas presenting in pregnancy.

Authors:  B M Smithers; C Welch; P Goodall
Journal:  Br J Surg       Date:  1986-07       Impact factor: 6.939

5.  Cystic tumors of the pancreas. New clinical, radiologic, and pathologic observations in 67 patients.

Authors:  A L Warshaw; C C Compton; K Lewandrowski; G Cardenosa; P R Mueller
Journal:  Ann Surg       Date:  1990-10       Impact factor: 12.969

Review 6.  Cystic pancreatic neoplasm in pregnancy: a case report and review of the literature.

Authors:  James E S Wiseman; Maki Yamamoto; Thang D Nguyen; Jeffrey Bonadio; David K Imagawa
Journal:  Arch Surg       Date:  2008-01

7.  Large mucinous cystadenoma of the pancreas during pregnancy: report of a case.

Authors:  Koichi Ishikawa; Teijiro Hirashita; Hideichiro Kinoshita; Motoo Kitano; Susumu Matsuo; Takashi Matsumata; Seigo Kitano
Journal:  Surg Today       Date:  2007-10-25       Impact factor: 2.549

Review 8.  Are pancreatic tumors hormone dependent?: A case report of unusual, rapidly growing pancreatic tumor during pregnancy, its possible relationship to female sex hormones, and review of the literature.

Authors:  G A Ganepola; A Y Gritsman; N Asimakopulos; A Yiengpruksawan
Journal:  Am Surg       Date:  1999-02       Impact factor: 0.688

9.  An extremely rare cause of acute abdomen in pregnancy: ruptured pancreatic mucinous cystadenocarcinoma.

Authors:  Selcuk Ozden; Berna Haliloglu; Erdin Ilter; Figen Temelli Akin; Abut Kebudi; Onder Peker
Journal:  Pancreas       Date:  2007-05       Impact factor: 3.327

10.  Pancreatic cystadenocarcinoma and pregnancy: a case report.

Authors:  C Baiocchi; G Landonio; M Majno; E Minola; F Scanzi; E Ghislandi
Journal:  Tumori       Date:  1990-06-30
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4.  Mucinous cystic neoplasms of the pancreas associated with pregnancy: Two case reports.

Authors:  Fernando Revoredo; José de Vinatea; Gustavo Reaño; Luis Villanueva; Fritz Kometter; José Arenas; Patricio M Polanco
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