Indian Journal of Orthopaedics

CASE REPORT
Year
: 2015  |  Volume : 49  |  Issue : 4  |  Page : 482--484

Multifocal bilateral xanthogranulomatous osteomyelitis


Rahul Sapra1, Pankaj Jain1, Shubha Gupta2, Rakesh Kumar1,  
1 Department of Orthopedics, S. M. S. Hospital, Jaipur, India
2 Department of Pathology, SDM Hospital, Jaipur, Rajasthan, India

Correspondence Address:
Rahul Sapra
Department of Orthopedics, S. M. S. Hospital, Jaipur, Rajasthan
India

Abstract

Xanthogranulomatous osteomyelitis is a rare chronic inflammatory disorder which clinically resembles bone tumor. It is characterized histologically by the presence of a large number of foamy histiocytes admixed with lymphocytes and plasma cells. Xanthogranulomatous inflammation can involve any organ, with kidneys and gall bladder being the worst affected. Only anecdotal cases of osteomyelitis have been reported in the past with scant medical literature. However, all the earlier reported cases, except one, were unifocal lesions. The authors present a case of multifocal xanthogranulomatous osteomyelitis involving the left medial malleoli, left talus and the right cuboid bones.



How to cite this article:
Sapra R, Jain P, Gupta S, Kumar R. Multifocal bilateral xanthogranulomatous osteomyelitis.Indian J Orthop 2015;49:482-484


How to cite this URL:
Sapra R, Jain P, Gupta S, Kumar R. Multifocal bilateral xanthogranulomatous osteomyelitis. Indian J Orthop [serial online] 2015 [cited 2020 Feb 28 ];49:482-484
Available from: http://www.ijoonline.com/text.asp?2015/49/4/482/159682


Full Text

 Introduction



Xanthogranulomatous inflammation, first reported in the genitourinary tract, can occur in many other organs such as the colon, appendix, pancreas, lymph nodes, gall bladder, salivary glands, endometrium, ovaries, fallopian tubes and the vagina. It may rarely affect lung, brain or the bone. Delayed type hypersensitivity reaction of cell mediated immunity has been implicated in its pathogenesis. Histologically, it is characterized by abundant foamy periodic acid-Schiff-positive histiocytes, containing abundant granular, eosinophilic cytoplasm in the initial stages, giant cells, fibrosis and calcification together with polymorphonuclear leukocytes, activated plasma cells and lymphocytes of polyclonal origin.

Bone involvement, although rare, generally mimics of bone tumor and all the earlier reported cases have been diagnosed only after biopsy. Radiographic picture is inconsistent and may show lytic or even blastic lesion with rare periosteal reaction, which makes preoperative diagnosis a challenge.

Xanthogranulomatous osteomyelitis is rare and only 11 cases have been reported so far [Table 1].{Table 1}

 Case Report



A 34-year-old male patient, farmer by occupation, attended the clinic with pain in his left ankle and the right foot since last 3 months. It was gradual in onset and increased at night. There was no history of trauma, fever or any significant past medical history. On examination, there was local rise of temperature with normal overlying skin and deep tenderness bilaterally. There was normal range of motion (ROM) at both the ankle and the subtalar joints with terminally painful movements. Laboratory investigations showed that total and differential leukocyte counts within normal range with raised erythrocyte sedimentation rate (38 mm at 1 st h). Serum calcium, phosphorus, parathormone, liver and renal function tests were found to be within normal range.

Anteroposterior and lateral radiographs showed a well defined lytic lesion in the medial malleoli and the talus on the left side and on the cuboid bone on the right side [Figure 1]. Bilaterally, there was no cortical breach, margins were selerotic, periosteal reaction or intralesional calcification was absent. Computed tomography findings were consistent with the X-ray features showing lytic lesions without cortical breach in the respective bones. Magnetic resonance imaging findings showed increased signal intensity on both T1- and T2-weighted images without any soft tissue extension of the lesion. With these features a probable diagnosis of benign bone tumor was made. Patient was taken for Jamshedi needle biopsy from the lesion. Yellow cheesy material (caseation like) was aspirated and sent for culture, AFB staining, polymerase chain reaction (PCR) for tuberculosis and histopathological examination. In the meantime, because of macroscopic findings of biopsy material and high prevalence of tuberculosis in our country, antitubercular treatment was started with isoniazid, rifampicin, pyrazinamide, and ethambutol emperically. However these drugs were stopped after 5 days because of a negative culture for other bacterias, AFB stain, PCR and histological picture consistent with xanthogranulomatous osteomyelitis. After a thorough review of literature at this stage, no definitive management protocol of the disease was found and the decision of curettage and bone grafting was taken. For left medial malleoli and right cuboid. Direct incision over the diseased areas were used. However, for left talus, anterolateral approach was used. Autogenic bone graft was taken from the right iliac crest. Curetted material was again sent for histopathological and microbiological assessment.{Figure 1}

On gross examination, the specimen consisted of multiple yellowish white tissue pieces. Histopathological examination on both the occasions revealed dense infiltration of lymphocytes, large number of plasma cells and abundant foamy histiocytes in islands and sheets [Figure 2]. Again no microorganisms were grown on culture and PCR study for Mycobacterium tuberculosis was negative. After 1.5 years of followup, patient is relieved of his symptoms. His visual analog scale score has improved from a preoperative value of 6 to a postoperative value of 2. There is no pre and postoperative loss of ROM. Followup X-rays show reasonably good incorporation of the bone graft without any signs of recurrence of the disease [Figure 3].{Figure 2}{Figure 3}

 Discussion



Xanthogranulomatous osteomyelitis has variable age of presentation occurring in adolescents to post menopausal women, according to previously reported cases. [1],[2],[3],[4],[5],[6] Except for the case described by Borjian et al. where they reported simultaneous lesions in the humerus and fibula, no other case report describes multifocal involvement. Furthermore, all of the previously mentioned cases have been reported in long bones namely femur, humerus, ulna, ribs, phalynx and tibia. [1],[2],[3],[4],[5],[6],[7],[8],[9] Involvement of small bones in the form of talus and cuboid makes this case unique. Borjian et al. and Kamat et al. isolated Staphylococcus aureus, while Cennimo reported Mycobacterium marinum from the lesion. However, no organism has been isolated in our case.

Differential diagnosis for xanthogranulomatous osteomyelitis includes Langerhan's cell histiocytosis, Erdhiem-Chester disease, lipid storage disorders such as gaucher's disease, chronic recurrent multifocal osteomyelitis, infiltrative storage disorder, malakoplakia, fibrohistiocytic tumor and metastatic renal cell carcinoma. [4] Being a farmer, fungal osteomyelitis was also considered as a possibility. However, presence of pathognomic cells in the form of foamy histiocytes on biopsy ruled out this possibility.

Differentiating between neoplastic process and inflammatory process remains the cornerstone in the management of this rare disorder. Unfortunately until date, only histopathological examination has shown promise in this regard. In the absence of any previously set treatment protocol for this disorder, the authors would like to recommend curettage with bone grafting as an effective method of treatment for this disease.

This rare entity should always be kept in mind as differential diagnosis by the treating surgeon and the radiologist.

References

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