CASE REPORT Annals of Nuclear Medicine Vol. 7, No. 1 57-60, 1993 Tc-99m-methylene diphosphonate (Tc-99m MDP) and Ga-67 concentration in soft tissue malignant fibrous histiocytoma (MFH) : Case report Toshiyuki KIDA,* Koji HOSHI,** Ryouichi HOSHINO,*** Yuji FUJITA,**** Shiro MUNAKATA**** and Masanobu YANAGISAWA***** * Department of Radiology, Honda Memorial Tohoku Cardio-Vascular Medical Center ** Department of Radiology, Fukushima Medical College *** Department of Orthopedics Koriyama National Hospital **** Department of Nuclear Medicine, Ohta Nishinouchi General Hospital ***** Department of Orthopedics, Fukushima Medical College A case of calcifying soft tissue malignant fibrous histiocytoma (MFH) which showed a concentration of Tc-99m MDP and Ga-67 citrate, is presented. Tc-99m MDP and Ga-67 citrate scintigraphies of the thigh mass were correlated with conventional radiography, computed tomography (CT) and angiography. Key words: malignant fibrous histiocytoma, Tc-99m-MDP, Ga-67-citrate, computed tomography, angiography INTRODUCTION NUMEROUS REPORTS in recent years have clearly established malignant fibrous histiocytoma (MFH) as a discrete pathologic entity.1-4 To the best of our knowledge, only a single case report of the bone and Ga-67 citrate scan findings of MFH has been published.4 Therefore, this case presents an additional example of concentrations of Tc-99m methylene diphosphonate (Tc-99m MDP) and Ga-67 citrate in MFH. In this paper, both Tc-99m MDP and Ga-67 citrate scintigraphy of the thigh mass are also correlated with conventional radiography, computed tomography (CT) and angiography. CASE REPORT A 66-year-old woman presented with a six month history of an enlarging painful left thigh mass. There was no associated weight loss, fatigue, or fever. Upon physical examination, a tender, firm, walnut-sized (3 x 5 cm), oval-shaped mass was found to be present medially in the middle of the left thigh. There were no overlying skin changes or local adenopathy. The conventional radiogaph of the left thigh showed only a soft tissue mass displacing the fat planes. A small, poorly defined area of calcifications was observed within the tumor mass (Fig. 1). There was no involvement of the underlying femur. The chest radiograph was normal. A Tc-99m MDP image showed intensely increased radiopharmaceutical accumulation in the mass, with the underlying femur having a normal scintigraphic appearance (Fig. 2). The remainder of the soft tissues and all of the osseous structures were normal on the whole body bone scan (Fig. 3). The Ga-67 scan demonstrated an ill-defined, moderately intensive accumulation in the mass (Fig. 4). Computed tomography demonstrated a clear delineation of the size and extent of the mass without any involvement of bone and its internal structure. The soft tissue mass had an attenuation coefficient which was similar to that of muscle. Calcifications were present in the mass (Fig. 5). Angiography revealed the mass to be supplied with blood by branches from the femoral artery. which was displaced and partially narrowed (Fig. 6). Numerous fine tumor vessels entered the mass and there was inhomogeneous intense capillary staining. The patient was treated with a wide en bloc local excision of the mass and reconstruction of femoral artery with vein graft. The gross pathologic examination revealed a well circumscribed margin with irregular central calcification (Fig. 7). The microscopic findings were diagnostic of MFH. DISCUSSION Malignant fibrous histiocytoma (MFH) is a soft tissue sarcoma of undifferentiated mesenchymal cell origin2 and is considered the most common soft tissue sarcoma in adults.3 It commonly occurs in the 5th and 6th decades with a 2: 1 male to female predominance. It most frequently occurs on the extremities and in the retroperitoneum, arising in the deep fascia or in the skeletal muscle. Approximately one third of all cases occur in the thigh, as illustrated in this case report. However, MFH has the potential of arising in any organ because of the ubiquitous presence of mesenchimal tissue.5 The imaging characteristics of MFH are typically nonspecific.8-11 In conventional radiography, MFH in the soft tissues appears as a nonspecific mass, usually measuring more than 5 cm in diameter.2 According to Mackey et al., none of their patients with FMH exhibited calcium deposition within the soft tissue mass and adjacent osseous involvement.4 However, tumor masses containing punctate calcifications have been observed by others.6 In our case, poorly defined calcifications were also seen within the tumor (Fig. 1). Both Tc-99m MDP and Ga-67 citrate scanning demonstrate intense accumulation of the radiopharmaceuticals in the tumor (Figs. 2, 4). There is no satisfactory explanation for the accumulation of both Tc-99m MDP and Ga-67 citrate. A variety of hypotheses5,7,8 have been invoked to explain the accumulation of these radiopharmaceuticals, but none of these has been definitely proved or disproved. In computed tomography, MFH is a predominantly dense muscle (Fig. 4). The attenuation coefficient is similar to that of muscle tissue and does not contain negative values, this being a point of difference from liposarcomas.9 The angiographic features of MFH are those of marked hypervascularity and early venous return (Fig. 6) and demonstrate fine, corkscrew-like tumor vessels with delayed emptying.10 Treatment for MFH is complete surgical removal by wide local excision. Operative planning requires a knowledge of the precise local extent, size and depth of the muscle and deep fascia, the location of its major feeding vessels, and the presence or absence of metastatic disease. Radioisotope scintigraphy, CT and angiography are techniques that can assist in planning the operation. Spatial resolution of bone and Ga-67 scintigraphies is certainly inferior to those of CT and angiography. However, we believe bone and Ga-67 scintigraphies are useful in the preoperative evaluation of patients with MFH, since detection of coexisting silent lesions is clearly important in planning treatment. Furthermore, we advocate the use of bone and Ga-67 scintigraphies for follow-up. REFERENCES 1. O'Brien JE, Stout AP: Malignant fibrous xanthomas. Cancer 17: 1445-1455, 1964 2. Weiss SW, Enzinger FM: Malignant fibrous histiocytoma: an analysis of 200 cases. Cancer 41: 2250 2266, 1978. 3. Kearney M, Soule E, Ivins J: Malignant fiborus histiocytoma: a retrospective study of 167 cases. Cancer 45: 167-178, 1980 4. Mackey JK, Alexieva-Jackson B, Fetters DV, et al: Bone and gallium scan findings in malignant fibrous histiocytoma: case report with radiographic and pathologic correlation. Clin Nucl Med 12: 17-21, 1987 5. Ros PR, Viamonte M, Rywlin AM: Malignant fibrous histiocytoma: mesenchimal tumor of ubiquitous origin. AJR 142: 753-759, 1984 6. Feldman F, Norman D: Intra- and extraosseous malignant fibrous histiocytoma (malignant fibrous xanthoma). Radiology 104: 497-508, 1972 7. Rosenthall L: Tc-99m-methylene diphosphonate concentration in soft tissue malginant fibrous histiocytoma. Clin Nucl Med 3: 58-61, 1978 8. Zazzaro PF, Bosworth JE. Schneider V, et al Gallium scanning in malignant fibrous histiocytoma. AJR 135: 775-779, 1980 9. Egund N, Ekelund L. Sako M, et al: CT of soft tissue tumors. AJR 137: 725-729, 1981 10. Burgener FA, Landman S: Angiographic features of malignant fibrous histiocytomas. Radiology 121: 581-583, 1976