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Published online before print December 2, 2002, 10.1148/radiol.2261011993
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(Radiology 2003;226:125-128.)
© RSNA, 2002


Vascular and Interventional Radiology

Osteoid Osteoma: Elevation of Cardiac and Respiratory Rates at Biopsy Needle Entry into Tumor in 10 Patients1

Daniel I. Rosenthal, MD, John J. A. Marota, MD, PhD and Francis J. Hornicek, MD, PhD

1 From the Departments of Radiology (D.I.R.), Anesthesia (J.J.A.M.), and Orthopedic Surgery (F.J.H.), Harvard Medical School, Massachusetts General Hospital, 199 Cambridge St, Boston, MA 02114. Received November 29, 2001; revision requested February 18, 2002; revision received March 21; accepted May 7. Address correspondence to D.I.R. (e-mail: dirosenthal@partners.org).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To evaluate changes in cardiac and respiratory rates in a consecutive series of patients who underwent percutaneous treatment for lesions presumed to be osteoid osteoma in whom general anesthesia was established.

MATERIALS AND METHODS: Changes in cardiac and respiratory rates were evaluated after establishment of stable general anesthesia in 14 patients who underwent needle biopsy and radio-frequency treatment. Cardiac and respiratory rates were recorded at penetration of skin, muscle, periosteum, cortex, and tumor. Treatment was performed before the biopsy report was available.

RESULTS: Biopsy results revealed osteoid osteoma in 10 patients, chondroblastoma in one, and a herniation pit in one. Results in the two remaining patients were nondiagnostic and were excluded. Puncture of skin, muscle, and periosteum caused no detectable change. However, in the 10 patients with biopsy-proved osteoid osteoma, puncture of the tumor caused the mean cardiac rate to increase an average of 26 beats per minute (40%) to 91 (range, 62–114; P < .001) and the mean respiratory rate to increase an average of 12 breaths per minute (50%) to a mean of 37 (range, 25–52; P < .001). These changes occurred within seconds of tumor puncture and were often the first indication to the surgeon that the tumor had been entered. In the two patients with other diagnoses at biopsy, no such change was apparent.

CONCLUSION: Mean cardiac and respiratory rates increase significantly at needle puncture of osteoid osteoma.

© RSNA, 2002

Index terms: Bones, biopsy, 40.1261, 40.3122 • Osteoma, 40.3122


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Osteoid osteoma is a small benign tumor of bone. Patients with this tumor are rarely pain free (1,2). More often the lesions cause pain that may be out of proportion to the small size of the tumor. The pain associated with osteoid osteoma is initially dull, throbbing, and intermittent and becomes more intense and knifelike over time. It may be exacerbated by physical activity and contact, such as palpation (3,4), but often occurs spontaneously. Patients frequently report that the pain is most intense at night, and it may wake them from sleep (5).

It is well-established that bone contains the neural elements required for transmission of nociceptive signals (6) and that these neural elements are present within trabecular and cortical bone and cancellous spaces (7,8). Despite these observations, there is a common misconception that all painful sensations arising from bone are a result of stimulation of the periosteum.

In the course of more than 200 percutaneous treatments of osteoid osteoma, we found that intensely painful stimuli arise from placement of a needle into the tumor itself. Our early attempts to perform this treatment by using local anesthetic were unsuccessful because of pain. Passage of a needle through skin, muscle, periosteum, and cortical bone does not have this effect. In our experience, this feature of osteoid osteoma is rarely seen in other entities and is almost never observed with malignant tumors. It may cause abrupt physiologic reactions in the patient, even during general anesthesia, that can be a cause of concern if not anticipated.

The purpose of this study was to evaluate changes in cardiac and respiratory rates in a consecutive series of patients who underwent percutaneous treatment for lesions presumed to be osteoid osteoma in whom general anesthesia was established.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Patients and Procedures
From March 2001 to December 2001, 14 consecutive patients (10 male and four female patients; age range, 4–43 years; mean age, 17 years) underwent needle biopsy and percutaneous radio-frequency treatment for lesions presumed to be osteoid osteoma. Clinical diagnosis was based on the history of pain unrelated to activity and the typical radiographic features of a rounded or oval lesion less than 15 mm in diameter surrounded by periosteal and endosteal sclerosis. All lesions were in the lower extremities.

Our study was approved by our institutional review board. After informed consent had been obtained, general anesthesia was induced with propofol (200 mg administered intravenously) (Gensia Sicor Pharmaceuticals, Irving, Calif). Then a laryngeal mask airway was positioned, and the patient was permitted to breathe Sevoflurane (1.5% inhaled) (Abbott Laboratories, North Chicago, Ill) and a nitrous oxide–oxygen mixture spontaneously. Neither narcotic nor nonsteroidal analgesics were administered prior to positioning of the biopsy needle within the lesion. The anesthetic concentration was maintained constant during the procedure. The area was not infiltrated with local anesthetic prior to the procedure.

A small hand-operated drill (Bonopty Bard; Radi Medical Systems, Uppsala, Sweden) was used to penetrate the cortex of the bone. The drill was advanced through periosteal and cortical bone with frequent computed tomographic (CT) monitoring until it was close to the tumor. It was then exchanged for a hollow bone biopsy needle (Osty-Cut; Bard/Angiomed, Karlsruhe, Germany) for tumor penetration. After biopsy, a radio-frequency electrode was introduced, and the tumor was heated to 90°C for 6 minutes by using our previously described methods (9).

Data Collection
Cardiac and respiratory rates were recorded throughout the procedure. The procedures were performed with CT monitoring, and each adjustment of the needle position was documented with an image. Since both the CT images and the cardiac-respiratory rate monitor were time-stamped, it was possible to relate the physiologic changes to the needle location. Particular attention was paid to these parameters when the skin and muscle were punctured, the periosteum was crossed, and the tumor was entered with the needle.

A biopsy sample was obtained in each case. However, the results were not available for several days; therefore, the procedure was performed without knowledge of the final histologic diagnosis.

Statistical Analysis
Differences in the mean cardiac and respiratory rates from baseline to peak values were analyzed by using commercially available statistical tools (Excel 97; Microsoft, Redmond, Wash). A two-sample t test for paired values with two tails was used. In addition, the Student t test for independent variables was used to compare the mean changes in cardiac and respiratory rates for the 10 patients with osteoid osteoma with those for the two patients with other diagnoses. A P value less than .05 was considered to indicate a statistically significant difference.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Biopsy results confirmed the diagnosis of osteoid osteoma in 10 cases. Two cases were nondiagnostic, although clinically consistent with osteoid osteoma, and were therefore excluded from further consideration. Of the other two, one case was interpreted as consistent with herniation pit of the femoral neck, and the other was a chondroblastoma (Table).


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Changes in Cardiac and Respiratory Rates after Needle Puncture in 12 Patients

 
In the 10 patients with osteoid osteoma, the mean baseline cardiac rate was 65 beats per minute (range, 51–73), and the mean baseline respiratory rate was 24 breaths per minute (range, 10–34) (Figure). In the two patients with other diagnoses, the baseline cardiac rates were 68 and 72, and respiratory rates were 24 and 25.



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CT images and tracings of cardiac rate (in beats per minute) and respiratory rate (in breaths per minute) during percutaneous radio-frequency treatment of an osteoid osteoma after establishment of general anesthesia. Times A, B, and C marked on the tracings correspond to the needle positions shown on CT images A-C, respectively. Notice that (A) soft-tissue penetration and (B) drilling through periosteum and cortical bone elicit no response, but (C) puncture of the tumor causes a sudden marked increase in cardiac and respiratory rates. H = hour, MIN = minutes.

 
Cardiac and respiratory rates did not change in any patient at the time of skin or muscle puncture. In six of 10 cases, the tumor did not involve the periosteal surface of the bone, and passage of the needle through the periosteum did not elicit any response.

In the 10 patients with osteoid osteoma, puncture of the tumor caused the mean cardiac rate to increase an average of 26 beats per minute (40%) to 91 (range, 62–114; P < .001) and the mean respiratory rate to increase an average of 12 breaths per minute (50%) to a mean of 37 (range, 25–52; P < .001). These changes occurred within seconds of tumor puncture and were often the first indication to the surgeon that the tumor had been entered.

In the two patients with other diagnoses, neither cardiac rate nor respiratory rate increased significantly.


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
On the basis of our experience, patients with osteoid osteoma exhibit sudden increases in cardiac and respiratory rates when the biopsy needle enters the tumor, but they show little or no reaction to the needle passing through skin, muscle, periosteum, and cortical bone.

A larger number of cases in the comparison group would be desirable. However, with the exception of osteoid osteoma, we perform most percutaneous procedures with local anesthetics. We believe that it would be difficult to interpret cardiac and respiratory changes in a patient who is awake; therefore, we are limited to the occasional instance in which osteoid osteoma is suspected but shown to be some other entity.

In a histologic study (10) of 18 osteoid osteoma specimens, nerve fibers were found in 16. Interestingly, one of the two cases without nerve fibers was from a rare example of a patient without symptoms. The authors believe that the nerves are sensitive to changes in vascular pressure, as are glomus tumors, and are the source of the pain that arises from the tumors.

Authors of a more recent study (11) used immunohistochemical methods that demonstrated the presence of nerves within both the tumor and the reactive tissues surrounding it. This feature appeared to be of diagnostic value, as it was not found in various other bone tumors including osteoblastoma, fibrous dysplasia, aneurysmal bone cyst, osteosarcoma, giant cell tumor, and chondroblastoma.

Pain sensations due to osteoid osteoma are probably mediated by prostaglandin release. High levels of prostacyclin and prostaglandin E2 have been found in cultured samples of tumor, and even in the urine of patients with tumors (12). Prostaglandin inhibitors such as nonsteroidal antiinflammatory medications usually block pain. Local features suggestive of inflammation (ie, bone marrow and periosteal edema, joint effusion) may simulate an inflammatory joint disorder (13). Some authorities (14) have suggested that the vasoactive properties of the prostaglandins result in pressure on unmyelinated nerves within the tumor to cause pain.

High concentrations of prostaglandins may be seen in other entities such as chondroblastoma, but in the absence of intratumoral nerves they do not cause the same pain pattern (15). We believe that our experience supports this interpretation. The rapidity of the response we have observed strongly suggests that nerves within the lesion mediate the process.

Pain originating from an osteoid osteoma may change over time. Initially described by many patients as dull and aching, it can become sharper and more intense over time (3). Some patients report intervals during which their pain is less severe. Over the course of years, the pain may diminish or even vanish despite the fact that the lesions still appear to be present at radiography (16,17). Not every patient experiences a marked response to penetration of the tumor. Perhaps those patients who do not experience exaggerated changes in cardiac and respiratory rates are in a different phase of the evolution of disease. An understanding of the frequency of this response would require evaluation in a larger group of patients; however, it is frequent enough that we now rely on it as an indication of successful needle placement.

On the basis of our experience, local infiltration of the soft tissues and periosteum with local anesthetics is not adequate analgesia for this procedure. Although spinal anesthetics are a good alternative for lesions of the lower extremities, they may require a longer recovery period and may not be appropriate for children, patients with certain back diseases, or those receiving anticoagulation therapy and nonsteroidal agents. When general anesthesia is used, the surgeon and anesthetist should be aware that painful stimuli that occur at the moment of tumor puncture can be much more intense than those that accompany other aspects of the procedure, and they must be alert to the possibility of patient movement.


    FOOTNOTES
 
Author contributions: Guarantor of integrity of entire study, D.I.R.; study concepts and design, D.I.R.; literature research, D.I.R.; clinical studies, F.J.H.; data acquisition, J.J.A.M., D.I.R.; data analysis/interpretation, D.I.R.; statistical analysis, D.I.R.; manuscript preparation, D.I.R., J.J.A.M., F.J.H.; manuscript definition of intellectual content, D.I.R.; manuscript editing, D.I.R., J.J.A.M., F.J.H.; manuscript revision/review and final version approval, D.I.R.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Jackson RP, Reckling FW, Mantz A. Osteoid osteoma and osteoblastoma. Clin Orthop 1977; 128:303-313.
  2. McDermott MB, Kyriakos M, McEnery K. Painless osteoid osteoma of the rib in an adult: a case report and review of the literature. Cancer 1996; 77:1442-1449.[CrossRef][Medline]
  3. Lichtenstein L. Osteoid-osteoma: bone tumors 3rd ed. St Louis, Mo: Mosby, 1965; 92.
  4. Mirra JM. Intraosseous tumors that produce osteoid woven, and/or lamellar bone In: Bone tumors: diagnosis and treatment. Philadelphia, Pa: Lippincott, 1980; 102.
  5. Cohen MD, Harringon TM, Ginsburg WW. Osteoid osteoma: 95 cases and a review of the literature. Semin Arthritis Rheum 1983; 12:265-281.[CrossRef][Medline]
  6. Houghton AK, Hewitt E, Westlund KN. Enhanced withdrawal responses to mechanical and thermal stimuli after bone injury. Pain 1997; 73:325-337.[CrossRef][Medline]
  7. Sherman M. The nerves of bone. J Bone Joint Surg Am 1963; 45:522-528.[Free Full Text]
  8. Fortier LA, Nixon AJ. Distributional changes in substance P nociceptive fiber patterns in naturally osteoarthritic articulations. J Rheumatol 1997; 24:524-530.[Medline]
  9. Rosenthal DI, Hornicek FJ, Wolfe MW, Jennings CL, Gebhardt MC, Mankin HJ. Percutaneous radiofrequency coagulation of osteoid osteoma compared with operative treatment. J Bone Joint Surg Am 1998; 80:815-821.[Abstract/Free Full Text]
  10. Schulman L, Dorfman HD. Nerve fibers in osteoid osteoma. J Bone Joint Surg Am 1970; 52:1351-1356.[Abstract/Free Full Text]
  11. O’Connell JX, Nanthakumar SS, Nielson GP, Rosenberg AE. Osteoid osteoma: the uniquely innervated bone tumor. Mod Pathol 1998; 11:175-180.[Medline]
  12. Ciabattoni G, Tamburrelli F, Greco F. Increased prostacyclin biosynthesis in patients with osteoid osteoma. Eicosanoids 1991; 4:165-167.[Medline]
  13. Alani WO, Bartal E. Osteoid osteoma of the femoral neck stimulating an inflammatory synovitis. Clin Orthop 1987; 223:308-312.
  14. Esquerdo J, Fernandez CF, Gomar F. Pain in osteoid osteoma: histological facts. Acta Orthop Scand 1976; 47:520-524.[Medline]
  15. Wold LE, Pritchard DJ, Bergert J, Wilson DM. Prostaglandin synthesis by osteoid osteoma and osteoblastoma. Mod Pathol 1988; 1:129-130.[Medline]
  16. Kneisl JS, Simon MA. Medical management compared with operative treatment for osteoid osteoma. J Bone Joint Surg Am 1992; 74:179-183.[Abstract/Free Full Text]
  17. Simm RJ. The natural history of osteoid osteoma. Aust N Z J Surg 1975; 45:412-415.[Medline]



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