Discussion
The fetal spleen develops during the 6th and 7th weeks from the aggregated reticular mesenchymal cells in the dorsal mesentery of the stomach. The fetal spleen contributes only to the production of the fetal megakaryocytes and thrombopoiesis.
Cystic lesions of the spleen occasionally develop within the spleen. The nonparasitic cysts are uncommon and of varying etiology. Postnatally the lesions are classified as true (primary) or false (secondary) cysts.
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The False cysts or pseudocysts have a fibrous capsule and may be post-traumatic, inflammatory or degenerative.
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The true splenic cysts, with a cellular layer, include vascular, serous, infectious, and congenital cysts and neoplasms (epidermoid, dermoid, hemangioma and lymphangioma). They usually have good prognosis [2].
Nevertheless 25 % of the splenic cysts are of unknown etiology [3].
The majority of splenic cysts are benign. They are not associated with fetal or infant compromise. Some cysts, however, can enlarge and can become symptomatic with a risk of post-traumatic rupture, hemorrhage and infection [3].
Prenatally the fetal spleen can be identified by ultrasound, and therefore cysts of the adjacent organs can be excluded. These lesions are usually diagnosed during the third trimester. Fetal spleen can be visualized by ultrasound from about 20 weeks of gestation. Okada and al report a case of splenic cyst observed as early as at 17 weeks of pregnancy. Yilmazer and Erden [5] described one case of the splenic cyst discovered at 31 weeks, which disappeared after seven months. Kabbra et al [7] described prenatal finding of the splenic cyst at 20 weeks of pregnancy.
Differential diagnosis
Several diagnoses may be considered when a cystic structure in the left upper abdomen of the fetus is found [8-10]:
Gastrointestinal cysts, such as choledochal and mesenteric cysts are preferentially located in the right and anterior part of the abdomen. The absence of septations can distinguish splenic cysts from duplication cysts. Renal cysts can be differentiated from splenic cysts by their topography related to the kidneys. Renal cystic dysplasia, hydronephrosis or obstructed duplication can be easily eliminated. Adrenal tumors may be cystic, but in this case they are heterogeneous in appearance. Ovarian cysts, pancreatic pseudocysts and mesenteric cysts are very rare. Omental cysts, choledochal cysts and left hepatic cysts are also very rare.
Management
Expectational management and surveillance can be recommended when a splenic cyst is found.
Garel at al [10] described seven cases of small, asymptomatic splenic cyst-like lesions diagnosed in fetuses and neonates [6-7]. None of these cysts were operated. Three of them completely disappeared.
Toddle at al [6] reported a case of prenatal diagnosis of the large left upper quadrant mass that was apparent at ultrasound at 32 weeks. Laparotomy was done at third day of life and a large splenic cyst (7 cm) was found in the lower pole of the spleen. Partial splenectomy was performed and no other cysts were found in other organs.
Conclusions
Published data and our experience indicate that an expectational management and surveillance can be recommended in the case of fetal splenic cysts. The vast majority of congenital splenic cysts disappear spontaneously during the first three month of life.
References
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2. Roth P., Clainquart N., Clerc-Bertin F., Teffaud O., Bawab F., Schaal J.P., Maillet R.- Diagnostic des masses kystiques abdominales du foetus. Med Foet Echo Gynecol 2000; N°42: 9- 20.
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5. Yilmazer Y.C., Erden A. Complete regression of a congenital splenic cyst. J Clin Ultrasound 1998; 26: 223-4.
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