Giant Joints in Association with Chronic Renal Failure

Tumoral Calcinosis (TC) is an uncommon benign entitiy characterized by solitary or multiple tumorlike densely calcified periarticular masses located typically in the extensor surfaces of the large joints. TC can be primary or secondary. The primary TC is a rare hereditary familial disorder of phosphate regulation. On the other hand, secondary TC is associated with an underlying disease, most frequently, chronic renal faliure (CRF). Herein, we present a case of 40 year old male patient with CRF and 10 years history of hemodialysis, presenting with swellings around the right hip and left shoulder joints. The diagnosis of secondary TC has been made with typical computed tomography (CT) and magnetic resonance imaging (MRI) findings. Secondary TC is an uncommon condition particularly occuring in association with CRF. Typical radiologic findings and clinical history are leading in the diagnosis and prevent unnecessary further evaluations.


Introduction
Tumoral Calcinosis (TC) is an uncommon benign condition characterized by solitary or multiple tumorlike periarticular/juxtaarticular depositions of calcium. Presentation occurs with solitary or multiple swellings typically located in the extensor surfaces of the large joints like hip, shoulder and elbow with less common involvement of knee and small joints [1]. TC can be primary or secondary. The primary TC is a rare hereditary familial disorder presenting in the first or second decade of life and it is further subclassified as primary hyperphosphatemic TC and primary normophosphatemic TC according to the underlying metabolic dysfunction of phosphate regulation [2, 3]. On the other hand, in secondary TC, there is an associated underlying disease causing multiple soft tissue calcifications, most frequently, chronic renal faliure (CRF) [3]. The underlying etiological mechanism for these massive periarticular calcifications in CRF is not clearly defined. Secondary hyperparathyroidism is suggested however, TC is also reported in the absence of secondary hyperparathyroidism [4]. Primary hyperparathyroidism, sarcoidosis, hypervitaminosis D and milk-alkali syndrome are among the other possible causes of secondary calcinosis [5]. We present a case of 40 year old male patient with CRF and 10 years history of hemodialysis presenting with secondary calcinosis of both hip and shoulder joints.

Case Presentation
A 40 year-old male patient with CRF who had been undergoing hemodialysis for 10 years had an abdominopelvic computed tomography (CT) scan 2 years before and a small soft tissue calcification was found incidentally around his right hip joint ( fig.1), which growed up to 10 cm without pain within 2 years. At that time, the lesion was a multilobulated, cystic, amourphous, densely calcified mass with multiple scattered fluidfluid levels ( fig. 2). There was no periosteal reaction or bony destruction. With history of CRF and typical CT features, the diagnosis of secondary TC was made. During this time another swelling around his left schoulder joint started to be grown up slowly without any symptom until the recently appeared pain which is aggrevated by movements of the joint. On magnetic resonance imaging [MRI], a periarticular soft tissue mass located in the subdeltoid bursa with the size of 14x11x8 cm was revealed. The lesion was heterogeneously hypointense on T1w and T2w images with scattered fluid-fluid levels ( fig. 3). The adjacent bones had normal signal intensity but, prominent perilesional soft tissue edema was present, which is probably the cause of recently appeared pain in the slowly growing lesion. This second lesion was also diagnosed radiologically as secondary TC and confirmed by histopathological evaluation. *Informed consent was taken from the patient.

International Journal of Clinical Case Reports and Reviews
Berrin Erok* AUCTORES Globalize your Research

Discussion
Secondary TC is an uncommon complication observed in patients with CRF, particularly in patients on hemodialysis with an incidence of 0.5%-1.2% [4,6]. TC has a cahracteristic appearance on radiological imaging studies. Radiography and CT scans show multilobulated, amorphous, cystic and calcified periarticular soft tissue masses typically located in a bursal distribution [3,7]. These cystic areas often demonstrate fluidcalcium levels on CT scans, which is caused by layering of milk of calcium and named also as sedimentation sign [8]. On MRI, TC show heterogeneous low signal intensity on T1w images. On T2w images, it may show low signal intensity pattern as would be expected from calcifications or may show bright, nodular pattern having heterogeneous areas of high signal intensity and signal voids. After IV gadolinium administration, some enhancement may be seen as a result of hypervascularity in the walls of the cystic areas [9]. In CRF patients, these masses typically grow slowly over months or years without pain, and may become symptomatic as a result of mass effect on adjacent tissues. Our case, presented with a recently appeared shoulder pain in the slowly growing lesion and perilesional edema/inflammation demonstrated on MRI, which is a very rare finding in association with TC. In the absence of bony destruction, the main differential diagnoses for soft tissue calcifications include metastatic calcifications which are associated with abnormal calcium and/or phosphate levels and dystrophic calcifications which are often secondary to trauma, underlying inflammatory processes like connective tissue diseases or atypical infections [3]. The big globs of calcifications near the joints in TC is differentiated from the metastatic and dystrophic calcifications which appear finely speckled calcifications throughout many other organs, such as kidneys, lungs, gastric mucosa, eyes, skin, vessels and also in joints. Although not expected from primary TC, osseous destruction and/or intraosseous penetration is a rare but possible challenging feature in some cases of secondary TC in CRF patients reported in the literature. Steinbach

Conclusion
Secondary TC is an uncommon condition particularly occuring in association with CRF. Typical radiologic findings and clinical history are leading in the diagnosis and prevent unnecessary further evaluations. However, the presence of some atypical features, if present, can be challenging while making the diagnosis and histopathological evaluation may be needed in equivocal cases.