Review Article | DOI: https://doi.org/10.31579/2640-1053/223
1Department of Pathological Anatomy, Arrazi Hospital, University Hospital of Mohammed VI - Marrakech/Faculty of Medicine and Pharmacy of Marrakech - Cadi Ayyad University Marrakech/Morocco
2Faculty of Medicine and Pharmacy of Guelmim – Ibnou Zohr University Agadir, Morocco
3Department of Neurosurgery, Ibn Tofail Hospital, University Hospital of Mohammed VI - Marrakech / Faculty of Medicine and Pharmacy of Marrakech - Cadi Ayyad University Marrakech/Morocco
4Department of Hematology, University Hospital of Mohammed VI - Marrakech/Faculty of Medicine and Pharmacy of Marrakech - Cadi Ayyad University Marrakech/Morocco
*Corresponding Author: Imane Boujguenna. Department of Pathological Anatomy, Arrazi Hospital, University Hospital of Mohammed VI - Marrakech / Faculty of Medicine and Pharmacy of Marrakech - Cadi Ayyad University Marrakech/Morocco.
Citation: Hind Rachidi, Imane Boujguenna, Halima El Khadraoui, Nawal Cherif Idrissi Guannouni, Ridouan Benelkhaiat et. al., 2024 , A 53-year-old female with pancreatic serous cystadenoma, J Cancer Research and Cellular Therapeutics, 8(8); DOI:10.31579/2640-1053/223
Copyright: © 2024, Imane Boujguenna. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received: 06 December 2024 | Accepted: 13 December 2024 | Published: 23 December 2024
Keywords: pancreas, serous cystadenoma, cystic neoplasm, case report
Serous cystadenoma of the pancreas is a cystic benign tumor composed of small cystic spaces lined by small cuboidal cells with clear cytoplasm. We report a new case of this entity in 53-year-old Moroccan woman, with no family history of tumor. She consulted for an abdominal pain revolving for 2 months. The clinical exam revealed an epigastric sensitivity with a general state preserved. An abdominal computed tomographic scan was performed and revealed the presence of multicyclic pancreatic tumor measuring 2.5x1.5. It was located in the isthmus of the pancreas. The patient had an isthmic pancreatectomy. Histologically the tumor was composed of variably sized cysts bordered by simple cuboidal, focally glycogen-rich epithelium. The stroma was variably collagenized and showed highly vascularized, delicate to broad fibrous septas. Thus, the diagnosis of primary serous cystadenoma of the pancreas was retained. Serous cystadenoma is an uncommon neoplasm that can be confused with malignancy.
Serous cystadenoma of the pancreas SCA is the most common benign tumor of the pancreas. It represents 1% to 2% of all pancreatic neoplasms [1]. These neoplasms have a predilection for older women two-thirds of patients are women [2]. They are often asymptomatic and discovered incidentally. Diagnostic criteria and growth potential, are not well specified and whose diagnosis is based on histology. The aim of this study is to discuss the clinical, histological features as well as the differential diagnosis.
We report the case of a 53-year-old woman. She had no history of pancreatitis, did not smoke, and did not drank alcohol. Family history was negative for pancreas, colon, ovarian, or breast cancer. She consulted for an abdominal pain revolving for 2 months. The clinical exam revealed an epigastric sensitivity with a general state preserved. prompting an abdominal ultrasound, which revealed a cystic lesion located at the level of the isthmus of the pancreas. This lesion measures 2.5X1.5cm. There were no focal liver lesions or any enlarged mesenteric or retroperitoneal lymph nodes. She then had an MRI/MRCP that showed a multiloculated cystic mass in the pancreatic isthmus measuring 2.5x1.5. The isthmic pancreatectomy was performed. The macroscopic study showed a multilocular cyst measuring 2.5x1.5cm. Microscopically a multi-cystic lesion is bordered by a regular simple cubic epithelium figure (1). It has an endothelium aspect per places. The cells lining the small cysts have clear cytoplasm, well-defined cytoplasmic borders, and small, round uniform nuclei with dense, homogeneous chromatin figure 2 The stroma was variably collagenized and showed highly vascularized, delicate to broad fibrous septas. the diagnosis retained is serous cystadenoma of the pancreas.

Figure 1: cystic lesion bordered by a regular simple cubic epithelium.

Figure 2: The cells have glycogen-rich clear cytoplasm, distinct cytoplasmic borders, and round, uniform nuclei with dense homogenous chromatin. Features of atypia or dysplasia are absent.
Cystic tumors of the pancreas are a benign epithelial neoplasm composed of uniform cuboidal, glycogen-rich cells, that often form cysts containing serous fluid OMS 2019. This entity presents 1-2% of pancreatic tumors, their diagnosis is important because their management depends on both clinical and imaging diagnoses [3]. Among these tumors, serous cystadenomas of the pancreas present about 20% of pancreatic cystic lesions [4]. These lesions have a strong female predilection 75% of cases. The mean age of the patients is 61.5 years [5]. About one third of the neoplasms present as an incidental finding at routine physical examination or at autopsy [6]. Approximately two thirds of patients exhibit symptoms related to local mass effects, including abdominal pain, palpable mass, nausea, vomiting, and weight loss. Jaundice due to obstruction of the common bile duct is unusual, even in neoplasms originating from the head of the pancreas. Pancreatic serum tumor markers are generally normal. Ultrasonography US and computed tomography CT reveal a multi-cystic tumor consisting of microcysts defined by their diameter less than or equal to 2 cm. cysts are readily separated by fibrous septa that can give in 30% of cases a central scar appearance, sometimes calcified [7]. More rarely, this lesion can take on a “honeycomb” appearance 20% or be visualized in an oligocystic form 10%, showing only a few cysts, with a diameter greater than 2 cm. Classic imaging aspects of SCAs are found in 20% of cases honeycomb appearance, calcifications, and central stellate scar [8]. In fact, in the largest study published, the SCAs may have an atypical presentation [2]. So SCA can be confused with other pancreatic cysts, including pancreatic neuroendocrine tumors, intraductal papillary mucinous neoplasms IPMN, and mucinous cystic neoplasms MCN. Thus, despite the availability of high-resolution radiologic techniques, a definitive preoperative diagnosis of SCA is still problematic. Treatment for pancreatic serous cystadenoma remains controversial. It is suggested that resection is generally carried out for symptomatic serous cystadenoma diameter> 4 cm, or tumors with rapid growth annual growth of greater than 4 mm, or the inability to distinguish a serous cystic neoplasm from a mucinous lesion, which has greater malignant potential. However, small or asymptomatic pancreatic serous cystadenoma should be provided with conservative treatment and close follow-up [5]. Macroscopically, Serous cystadenomas of the pancreas are single, well-circumscribed, slightly bosselated, round lesions, with diameters ranging from 1-25 cm in greatest dimension average, 6-10 cm. On section, the neoplasms are sponge-like and are made up of numerous tiny cysts filled with serous clear watery fluid. The cysts range from 0.01-0.5 cm, with a few larger cysts of up to 2 cm in diameter. Often, the cysts are arranged around a more or less centrally located, dense fibronodular core from which thin fibrous septa radiate to the periphery central stellate scar. Histologically, small cystic spaces lined by small cuboidal cells clear cytoplasm glycogen, minimal mucin, myoepithelial layer present, round hyperchromatic central nuclei. The serous cystadenoma has characteristic imaging and histologic features that may differentiate it from other potentially malignant cystic tumors such as mucinous cystic tumors and intraductal papillary mucinous neoplasms [9, 10].
SCAs of the pancreas are becoming increasingly more frequent because of advances in imaging techniques. These lesions often present with classic imaging findings across multiple modalities that help to distinguish them from other cystic tumors. A correct diagnosis is important in order to give a specific treatment and prognosis.
The authors declare that they have no conflicts of interest.
Authors' contributions:
All authors contributed to the writing of this manuscript.
Consent to publication:
Written informed consent has been obtained from the patient for the publication of this case report and all accompanying images. A copy of the written consent is available for review by the editor-in-chief of this journal.
Financing:
The authors did not receive any specific funding for this study.
Dear Editorial Team, Clinical Medical Reviews and Reports. My experience with the journal was highly positive. The peer-review process was rigorous, constructive, and completed in a timely manner. The reviewers provided valuable comments that helped improve the quality and clarity of our manuscript. The editorial office was professional, responsive, and supportive throughout all stages of the publication process. Communication was clear and efficient, and any questions were addressed promptly. Overall, I found the journal to maintain high scientific standards and an excellent publication workflow. I would be pleased to consider submitting future work to this journal. Best wishes from, Elena Popa.
It was my pleasure to submit my testimonial concerning the Reviewer Board of our Scientific Journal “Brain and Neurological Disorders”. The Reviewers focused on some modifications and their contribution was helpful. The ladies of our Editorial Office were also supported my efforts. It was my honor to have such a co-operation and I am looking forward for more collaboration.
Dear Grace Pierce, Editorial Coordinator of Journal of Clinical Research and Reports, Thank you for the speedy and efficient peer review process. I appreciate the fact that your peer reviewers do not take months to respond like with some other journals. I would also like to thank the editorial office for responding quickly to my questions. It is an excellent journal. I plan to submit more manuscripts in the future. Best wishes from, Robert W. McGee
Dear Grace Pierce, Editorial Coordinator of Journal of Clinical Research and Reports, Working with you and your team on our recent publication in JCRR has been a truly wonderful and enjoyable experience. The responses were prompt, and the reviewers were patient, constructive, and highly professional. One reviewer in particular gave me the feeling that a professor was carefully reading and commenting on my coursework, which was deeply touching. The entire process was straightforward and hassle‑free, with no tedious online forms to complete. I highly recommend this journal. Best wishes from, DR Aibing Rao, Head of R&D
I Appreciate the Opportunity to Share my Experience with the Journal of Clinical Research and Reports. The peer review process was timely and constructive, and the feedback provided helped improve the quality of our manuscript. The editorial office was professional, responsive, and supportive throughout the process, ensuring smooth communication and efficient handling of the submission. Overall, it was a positive experience collaborating with your team.
Dear Mercy Grace, Editorial Coordinator of Obstetrics Gynecology and Reproductive Sciences, We would like to express our gratitude for your help at all stages of publishing and editing the article. The editors of the magazine answer all the necessary questions and help at every stage. We will definitely continue to cooperate and publish other works in the Obstetrics Gynecology and Reproductive Sciences! Best wishes from, Alla Konstantinovna Politova,