We present a case of a 44-year-old female who was evaluated for left recurrent flank and abdominal pain. Abdominal ultrasonography demonstrated a large cystic mass on the upper pole of the left kidney. Magnetic resonance imaging showed a large, homogenous cystic mass measuring
Adrenal cystic lesions are rare and mostly identified incidentally during radiological investigations or at surgery for unrelated reasons. Its incidence in autopsy series varies between 0,064 and 0,18%. Adrenal cysts are histologically classified into four main groups: endothelial cysts (45%), pseudocysts (39%), epithelial cysts (9%), and parasitic cysts (%7). Endothelial cysts are divided into two subgroups: lymphangiomatous and angiomatous cysts. Lymphangiomatous adrenal cysts are also known as adrenal lymphangioma (AL) [
We report a case of an AL, which is mimicking a renal cyst, with an emphasis on the symptoms, differential diagnosis, and treatment.
A 44-year-old female presented to the outpatient clinic with left recurrent flank and abdominal pain during the last 5 years. On physical examination, she was relaxed with palpation of the abdomen and was known to have a stabile hypertension and panic attack diseases. On laboratory evaluation, a normal urine analysis and normal hemoglobin, urea, and creatine levels were identified. Abdominal ultrasonography (US) demonstrated a large cystic mass on the upper pole of the left kidney. Magnetic resonance imaging (MRI) showed a large homogenous cystic mass measuring
T1-weighted MRI image of adrenal lymphangioma in coronal section.
According to clinical and radiological findings, surgical excision was carried out with a subcostal flank incision. A cystic mass, approximately 10 cm in diameter, was identified on the suprarenal area without a distinct plan between left kidney and adrenal gland; therefore, the cyst was excised with a small part of the left adrenal gland without any intraoperative complications. Macroscopically there were osseous and cartilage-like tissues partly on the surface of the cyst wall. The cyst was filled with clear, nonviscous, brown colored fluid. After a 3-day hospital stay, the patient was discharged and the postoperative course was uneventful.
Histologically, the cyst showed a typical multicystic architecture with dilated spaces lined by flattened, bland, simple lining. The cystic spaces occasionally contained proteinaceous material, lacking red blood cell content, and the cyst wall contained adrenal cortex (Figure
Multicystic architecture with dilated spaces lined by flattened lining cells (HE
The flattened cells lining the cyst stained positive for D2-40 (
AL is a benign vascular lesion and a subtype of endothelial adrenal cysts. The first case of AL had been reported in 1965 and recently less than 50 immunohistochemically proven cases have been reported in the literature [
The etiology and pathogenesis of AL are still unknown and matters of debate. The most favored theories are: malformation of lymphatic channels, ectasia of lymphatic channels, obstruction of proximal lymphatic channels, and a cystic degeneration in a hamartoma [
ALs are macroscopically multilocular, thin-walled cystic lesions and are filled with nonviscous, clear, yellow-brown-colored fluid. Histologically, they are multicystic lesions formed by irregular dilated spaces lined with flattened, simple endothelial cells. Endothelial atypia has never seen in any of the lesions in the literature [
ALs are usually asymptomatic. If they are symptomatic, symptoms are usually related to the mass effect and position of the cyst. The most common symptoms are abdominal or flank pain, gastrointestinal disturbance, palpable mass, headache, and arterial hypertension and palpitation especially in functional cysts [
The majority of the adrenal cysts are benign and non-functional. Neri and Nance reported 6 adrenal cyst cases of their own and reviewed over 600 cases, in which they detected that the malignancy incidence was 7% [
On US, AL is a well-marginated, anechoic, cystic lesion typically located on the suprarenal area. There can be acoustic shadows and internal echoes, if calcifications or internal debris are present [
In our case, MRI confirmed that the cystic mass were appeared that a part of the left kidney without a distinct plane between the kidney and the adrenal gland, so it was concluded that the the cyst originated from kidney rather than adrenal gland. We decided to resect the cyst surgically because of its large size and bothersome pain to the patient. To our knowledge, this is the unique case of an AL considered as a renal cyst because of its radiological appearance. But there are examples of misdiagnosis of other type of adrenal cysts in the literature [
The subject of debate is which cysts need surgical intervention and which cysts need to be treated conservatively. The management of adrenal cysts and indications for surgery have to be based on oncological, endocrinological and clinical findings: (1) oncological indications: large cysts (5 cm or more in diameter), high density on unenhanced CT (>10 HU), delayed wash-out of the contrast medium, significant growth of the cyst on serial imaging, (2) Functional cysts, (3) Symptomatic cysts and cysts which can cause complications such as hemorrhage, rupture, or infection [