Osseous Kaposi's sarcoma

Clinical Cases 03.03.2003
Scan Image
Section: Musculoskeletal system
Case Type: Clinical Cases
Patient: 35 years, male
Authors: L. Thanos, V. Kalioras, S. Mylona, E.Despotopoulos, N. Batakis
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AI Report

Clinical History

HIV-positive patient with an osteolytic lesion.

Imaging Findings

This patient, who had been HIV-positive for 8 years and suffered from cutaneous Kaposi's syndrome for 6 years, underwent chemotherapy (ABV-HCG) and radiotherapy (3500rads). The lesions were located on the chest, left arm, left thigh and left calf. In May 2000, the cutaneous lesions worsened, with redness and painful swelling of the patient's left arm in the region of his elbow. X-rays showed a large osteolytic lesion of the ulna, and so regional radiotherapy and systematic chemotherapy were begun.

In Septemper 2001, the patient presented with right-sided chest pain. Dual-phase CT of the thorax was performed, and showed a large mass of soft tissue at the back wall of the thoracic cavity, accompanied by osteolytic lesions of the ribs and the vertebrae next to it. There was and extension into the spinal canal. Other, oval-shaped osteolytic lesions with soft tissue masses next to them, were seen on the right side of the chest wall and the left side of the sternum. Lymph-node enlargement was noted at the mediastinum and axillae, especially on the left side. Osteolytic lesions with adjacent soft tissue mass, also occurred on the right side of the sacrum and acetabulum, as CT of that region showed.

In October 2001, core needle biopsy of the mass under CT guidance was performed and pathoanatomic result was "Kaposi's sarcoma". Appropriate therapy was instituted.

In February 2002, CT of the thorax and abdomen was performed to establish the patient's response to the therapy. The osteolytic lesions of the ribs and the vertebrae, seemed to be a little smaller. The lymph nodes of the mediastinum and axillae were smaller as well. The osteolytic lesion at the sacrum was unchanged.

Discussion

Kaposi's sarcoma (KS) is a multifocal neoplasm thought to arise from lymphatic endothelial cells. Histologically, KS is characterised by a proliferation of spindle cells and cleft-like vascular structures. It is the most common neoplasm occurring in HIV-positive patients. It is usually aggressive involving many organs, although skeletal disease is rare. Bone involvement is seen most commonly as invasion of bone from adjacent skin lesions (infiltrative cutaneous or mucosal KS). Primary bone lesions, without involvement of the overlying skin are very rare.

Radiologically, bone KS appears as a periosteal reaction, cortical erosions or as osteolysis. Irregular cortical erosions are most typical, and are probably due to KS arising in the cortex or periosteum. Erosions may also occur secondarily, as a result of external pressure from nodules in the surrounding soft tissue but, in this case, they appeared as smooth lesions. Osteolysis can present as uniform rarefaction, cystic lesions, or almost-complete bone destruction. The possibility of new bone formation with minimal osteoblastic changes has been described in a few instances. These lesions are probably related to the production and release by KS cells of cytokines such as interleukin-1 and interleukin-6, which can stimulate bone resorption, in part by increasing osteoclast development and function. In addition, the pressure generated by enlarging KS nodules may induce resident monocytes to produce cytokines that, in turn, trigger osteoclast activation.

CT scanning more precisely identifies lytic bone changes and MR imaging shows marrow abnormalities similar to those in lymphoma and infection. Soft tissue masses are again more easily identified on MR imaging than CT scanning. Nuclear medicine studies may be useful for further evaluation. Red blood cell pooling in cutaneous lesions can be seen with technetium 99m MDP scans. Combined thallium-201 and gallium-67 imaging reveals a characteristic pattern of uptake with thallium-201, but not with gallium-67. Infection and other neoplasms, such as lymphoma, are typically gallium avid. Nevertheless, biopsy may be necessary for definitive diagnosis.

Differential Diagnosis List

Osseous Kaposi's sarcoma

Final Diagnosis

Osseous Kaposi's sarcoma

Liscense

Figures

Osseous Kaposi's sarcoma

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Osseous Kaposi's sarcoma
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Osseous Kaposi's sarcoma
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Osseous Kaposi's sarcoma
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Osseous Kaposi's sarcoma
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Osseous Kaposi's sarcoma