Splenic lymphangiomas as a common indication for splenectomy: a case series with literature review

We report from a Subsaharan African country a series of patients that underwent total splenectomy for a variety of diseases. Open surgery was performed in almost all cases (15/16 patients, 93.75%); SCD (5/16 cases, 31.25%), SL (4/16 cases, 25%) and malignant intra-abdominal tumors with suspected extension to the spleen (4 cases, 25%), were the most indications for the splenectomy. Benign splenic conditions were the most frequent indications for surgery (12/16 patients, 75%), among them SCD (5/12 cases, 41.66%) and SL (4/12 cases, 33.33%) were the leading causes of surgery. Hematologic diseases have been reported to be the major indication for splenectomy in the literature [17, 21‐28], however we are not aware of SL as a common indication for surgery even in selected series (especially in pediatric population). The small sample and the short period of our study could be the reason of these discrepancies with the previous reports in the literature. Hematologic diseases such as idiopathic thrombocytopenia purpura (ITP) and hereditary spherocytosis are the major indication for splenectomy in series especially from Western countries [21‐23, 25] while splenic complications of SCD represent a common cause of splenectomy in African and Middle-East countries [16, 29, 30]. Splenectomy is usually performed in patients with SCD complications like acute splenic sequestration crisis, hypersplenism, splenic abscess, and massive splenic infarction, with good outcomes and this surgery also reduces requirements for repeated blood transfusions and prevents mechanical complications of an enlarged spleen [16, 30]. However, a recent meta-analysis challenged these beneficial effects of splenectomy by concluding that there is a lack of evidence from trials showing that splenectomy improves survival and decreases morbidity in people with SCD [31]. Malignant tumors either primary or secondary affect very rarely the spleen, and represent a less usual indication for splenectomy [23, 32]. In our series there were no primary splenic tumors, however we have registered 3 cases with splenic capsular invasion by cancers from adjacent organs (stomach and left colon).

Since its introduction in surgical clinical practice in early 1990 s, laparoscopic splenectomy (LS) has become a gold standard in the management of patients with splenic diseases either benign or malignant [21, 23, 25]. Many reports shows that LS has lower morbidity with cosmetic advantages, less perioperative bleeding, short hospital stay and less conversion rate to open surgery [23, 33]. Even in patients with massive splenomegaly (> 1000 g), LS could be safely performed [33, 34]. However, this minimally invasive surgery requires experience and acquisition of more technical skills over time (learning curve), with longer operative time especially in patients with massive splenomegaly [23, 25, 35]. In our series, open splenectomy (OS) was widely performed (15/16 cases, 93.75%) even in patients with benign diseases and mild splenomegaly (< 500 g). The reason for this classic surgical approach was the lack of adequate laparoscopic materials in our hospitals, with rare surgeons that have skills in laparoscopic surgery.

In our study, patients with SL were older than patients with other benign splenic conditions (mean age of 28.25 versus 20.87 years), because of many children with SCD in this subgroup of benign splenic conditions. Also, patients with SL presented with heavier spleens and massive splenomegaly (mean weight and size of 1675 g and 19.62 cm) whereas patients with other benigh splenic conditions had mild splenomegaly (mean weight and size of 418.75 g and 14.43 cm). In fact in this subgroup, the indications for splenectomy were acute symptoms such as abdominal pain, fever and hypersplenism, rather than the importance of the splenomegaly and abdominal distension in comparison with patients that had SL.

In the literature, SL are usually reported in children as asymptomatic or rarely symptomatic lesions, with few case reports in adults [2, 4, 6, 7, 15, 36]. Our current series challenged these classic features as all patients presented with massive splenomegaly with abdominal distension (mean splenic weight of 1675 g, range of 1300–2300 g). Also, in our series patients were older (mean age of 28.25 years, range of 17–37 years) with 3 young adults and 1 adolescent patient of 17 years. As in our cases, SL present as cystic lesions of variable size with honeycombing appearance and compact pale, yellowish content (lymphatic fluid) on resected specimens [2, 7]. The preoperative imaging techniques are not specific, they show only the cystic aspect of the lesion, that could correspond to a variety of cystic splenic lesions [12]. The Table 3 summerises the main characteristics of splenic cystic lesions. Several classifications of splenic cystic lesions have been proposed [6, 13, 15, 36]. Splenic cystic lesions are classified as: neoplastic cysts, congenital epithelial cysts (CEC), parasitic cysts (mainly hydatid cysts), and other cysts as a results of infarction (traumatic cysts) or inflammation/infection (abscess). Neoplastic cysts include vascular lesions (hemangiomas, lymphangiomas or angiosarcomas) or any malignant solid splenic tumors with cystic degeneration. Vascular cystic lesions are lined by regular flat endothelial cells, with luminal content made of red blood cells (hemangioma) or proteinaceous amorphous eosinophilic material (lymphangioma) [36]. The histological aspects of our 4 cases of SL were typically consistent with the later aspect. In angiosarcomas, the lining endothelial cells present atypias, mitoses and necrosis [37]. Congenital epithelial cysts (CEC) are common in pediatric population, the cysts are lined by epithelial cells with mesothelial, transitional or squamous differenciation. All these types of epithelial cells could be found in combination in a single lesion. These lesions are supposed to derive from mesothelial invagination through the splenic parenchyma [6, 15]. Splenic hydatid cysts are caused by Echinococcus granulosus infection and are endemic in certain areas of the World [38]. On histopathological analysis, the parasit’s structures are readily observed in the splenic cyst. The remaining causes of splenic cysts are the result of previous trauma, infarction or infection. They present histologically as pseudo-cystic lesions without epithelial or endothelial lining. Previously, splenic pseudo-cysts were believed to be common, however a careful histological analysis usually find focal endotheilal or epithelial lining in what may be misdiagnosed as a pseudo-cyst [14].

As a retrospective analysis, our study has some limitations, especially a small number of patients. The data about imaging techniques and follow-up are not available. However some provisional conclusions could be drawn, until the availability of larger studies on SL in the future.