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2.
Acta Cytol ; 42(3): 697-702, 1998.
Article in English | MEDLINE | ID: mdl-9622690

ABSTRACT

OBJECTIVE: To compare the diagnostic sensitivity and specificity of fine needle aspiration (FNA) to those of needle core biopsy (NCB) and to attempt to determine if a complementary role exists for the two modalities. STUDY DESIGN: Skeletal lesions in 144 patients were evaluated with concomitant FNA and NCB over a 21-year period. FNAs and NCBs were divided as diagnostic of neoplasm, normal or inflammatory (i.e., osteomyelitis), or unsatisfactory. The results of each modality were then reviewed and compared. RESULTS: In the 144 total cases, a diagnosis was possible in 79% (114) cases. FNA and NCB concurred in 73% (83) of diagnostic cases. Concurrence was 87% between diagnostic FNA (83) and NCB (95). The two modalities agreed in 78% of cases diagnosed as metastatic carcinoma and in 59% of primary malignant tumors of bone (17) (excluding Ewing's sarcoma). FNA alone was diagnostic in 8% (9) of cases, including 5 metastatic carcinomas, 2 chondrosarcomas, 1 Ewing's sarcoma and 1 case of osteomyelitis. This represented 24% of the 38 cases in which NCB was unsatisfactory (11) or normal (27). NCB alone was diagnostic in 19% (22) of cases, including 11 metastatic carcinomas, 3 osteosarcomas, 1 chondrosarcoma, 1 spindle cell sarcoma (not otherwise specified), 1 Ewing's sarcoma, 2 capillary hemangiomas and 3 cases of osteomyelitis. This represented 43% of the 51 cases in which FNA was misinterpreted (2), unsatisfactory (33) or normal (16). NCB more specifically typed a metastatic lesion or suggested a primary focus in 21% (12) of the 58 cases in agreement. It also more specifically subtyped 50% (5) of the 10 primary malignant tumors of bone. CONCLUSION: Given these findings, NCB is more specific in the evaluation, grading and typing of skeletal lesions in particular malignant primary bone tumors. Overall, there is excellent agreement between FNA and NCB, especially in the evaluation of benign primary bone tumors. Most important, FNA improved the diagnostic yield in 24% of cases when NCB was normal or unsatisfactory, obviating the need for rebiopsy. FNA should be performed concurrently with NCB in the evaluation of skeletal lesions since the two modalities are complementary.


Subject(s)
Biopsy, Needle/methods , Bone Neoplasms/diagnosis , Bone and Bones/pathology , Tomography, X-Ray Computed , Adolescent , Adult , Aged , Aged, 80 and over , Bone Neoplasms/pathology , Bone Neoplasms/secondary , Child , Child, Preschool , Diagnosis, Differential , Evaluation Studies as Topic , Female , Humans , Infant , Male , Middle Aged , Osteomyelitis/diagnosis , Osteomyelitis/pathology , Predictive Value of Tests , Retrospective Studies , Sensitivity and Specificity , Suction
3.
J Surg Oncol ; 67(4): 255-60, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9579374

ABSTRACT

BACKGROUND AND OBJECTIVES: Metastatic disease represents the most common neoplastic process involving bone. Recently, a small subset of cortical based metastatic lesions has been identified. We attempted to delineate the incidence, origin, location, and possible significance of these lesions within an orthopaedic patient population. METHODS: A chart and radiographic review of patients treated for metastatic disease to bone over a 17-year period was performed. Inclusion criteria for lesions were as follows: 1) an appendicular skeletal site, 2) histopathologic confirmation of origin, and 3) presence within a patient diagnosed with a single, known neoplastic process. The lesions were classified as either cortical or medullary based. RESULTS: Eighty-three lesions (70 patients) satisfied inclusion criteria. Most lesions were of pulmonary (26), breast (22), renal (16), or prostatic (8) tumor origin. Eighteen lesions (22%) from 15 patients were identified as cortical and represented initial presentation in 7 patients. These lesions were of pulmonary (11), renal (5), and breast (2) tumor origin. CONCLUSIONS: Cortical based metastases within the appendicular skeleton may occur more frequently than previously expected. While tumors of pulmonary and renal origin accounted for 42 of the 83 (51%) appendicular lesions, they were responsible for 16 of the 18 (89%) cortical metastases. This preponderance of pulmonary and renal metastases to the cortex is consistent with previously published reports. Our findings may be of value when diagnosing and treating patients whose initial presentation is a cortically based lesion.


Subject(s)
Adenocarcinoma/secondary , Bone Neoplasms/secondary , Neoplasms, Unknown Primary/pathology , Adenocarcinoma/diagnostic imaging , Adolescent , Adult , Aged , Aged, 80 and over , Bone Neoplasms/diagnostic imaging , Breast Neoplasms/pathology , Child , Child, Preschool , Female , Femoral Neoplasms/diagnostic imaging , Femoral Neoplasms/secondary , Humans , Infant , Kidney Neoplasms/pathology , Lung Neoplasms/pathology , Male , Middle Aged , Prostatic Neoplasms/pathology , Radiography
4.
J Clin Oncol ; 15(1): 76-84, 1997 Jan.
Article in English | MEDLINE | ID: mdl-8996127

ABSTRACT

PURPOSE: The specific aims of this study were to improve event-free survival (EFS) in patients with newly diagnosed nonmetastatic osteosarcoma of an extremity using the histologic response to neoadjuvant chemotherapy to determine postoperative chemotherapy; to evaluate a uniform histologic grading system that measures tumor response; and to identify patient characteristics that might influence EFS and survival. PATIENTS AND METHODS: Two hundred sixty-eight patients with nonmetastatic osteosarcoma of the extremity were entered between August 1983 and October 1986. Preoperative chemotherapy consisted of four courses of high-dose methotrexate (MTX) and one course of bleomycin, cyclophosphamide, and dactinomycin (BCD). Histologic response to preoperative chemotherapy was determined by morphometric analysis. Good histologic responders (< 5% residual viable tumor) were treated postoperatively with MTX, BCD, and doxorubicin (DOX); poor histologic responders were treated with BCD, DOX, and cisplatin (CDDP). RESULTS: The 8-year EFS and survival rates were 53% and 60%, respectively. Two hundred six patients had their tumors assessed for histologic response: 28% displayed a good histologic response to preoperative chemotherapy. Good histologic responders had an 8-year postoperative EFS rate of 81% and survival rate of 87%; those with a poor histologic response had an 8-year postoperative EFS rate of 46% and survival rate of 52%. A primary tumor site in the proximal humerus or proximal femur and an elevated serum alkaline phosphatase level were associated with an increased risk of an adverse event, whereas the type of surgical procedure was not. CONCLUSION: EFS and survival appear to be directly related to histologic response to neoadjuvant chemotherapy.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bone Neoplasms/drug therapy , Extremities , Osteosarcoma/drug therapy , Adolescent , Bleomycin/administration & dosage , Bone Neoplasms/pathology , Bone Neoplasms/surgery , Chemotherapy, Adjuvant , Child , Cyclophosphamide/administration & dosage , Dactinomycin/administration & dosage , Disease-Free Survival , Humans , Methotrexate/administration & dosage , Osteosarcoma/pathology , Osteosarcoma/surgery , Vincristine/administration & dosage
5.
Clin Orthop Relat Res ; (331): 277-82, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8895650

ABSTRACT

Primary retroperitoneal sarcomas may present with symptoms and signs that mimic common musculoskeletal disorders of the extremities that are quite remote from the source of the problem. This often misleads the clinician and results in delays in diagnosis. The authors present 6 patients with retroperitoneal sarcoma who had a common or nonspecific orthopaedic condition of the extremity. Delays in diagnosis ranged from 2 to 30 months. No patient survived his or her tumor. Clinicians should be alerted to the possibility of a retroperitoneal tumor that presents primarily or initially with extremity signs and symptoms but with few or no clues of the presence of a localized sarcoma in the retroperitoneal space.


Subject(s)
Musculoskeletal Diseases/diagnosis , Retroperitoneal Neoplasms/diagnosis , Sarcoma/diagnosis , Adult , Aged , Child , Combined Modality Therapy , Diagnosis, Differential , Diagnostic Errors , Female , Humans , Leg , Male , Middle Aged , Retroperitoneal Neoplasms/therapy , Sarcoma/therapy
7.
J Bone Joint Surg Am ; 78(8): 1172-80, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8753709

ABSTRACT

The clinical features, radiographic and histopathological findings, treatment, and results are described for eleven patients who were managed for an extracranial osteoma at our medical center between 1980 and 1993. Ten of the patients were initially seen because of dull, aching bone pain that had been present for two weeks to thirty years. Radiographs demonstrated single or multiple homogeneous, well defined, radiodense foci with smooth round or lobulated margins. The histopathological features consistently included uniformly dense, compact, cortical-like, mature lamellar bone. The preoperative diagnosis was unclear for all patients, and osteoma was rarely considered in the differential diagnosis. For four patients, a tentative diagnosis of osteosarcoma was made, and a wide excision was carried out in two of these patients. Marginal excision with less than three millimeters of normal tissue around the lesion was performed in most patients. None of the osteomas recurred, and ten patients had relief of the pain. Awareness of the clinical, radiographic, and histopathological features of osteoma, as described, is valuable for making a differential diagnosis and for distinguishing osteomas from other lesions.


Subject(s)
Bone Neoplasms/therapy , Osteoma, Osteoid/therapy , Osteosarcoma/therapy , Adolescent , Adult , Bone Neoplasms/diagnostic imaging , Bone Neoplasms/pathology , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Osteoma, Osteoid/diagnostic imaging , Osteoma, Osteoid/pathology , Osteosarcoma/diagnostic imaging , Osteosarcoma/pathology , Tomography, X-Ray Computed
10.
Semin Arthroplasty ; 5(2): 76-84, 1994 Apr.
Article in English | MEDLINE | ID: mdl-10147347

ABSTRACT

Twenty-five patients had a procedure consisting of resection of the distal femur or proximal tibia for aggressive or malignant neoplasms. The resulting bony gap was bridged by allografts averaging 18 cm in length. Fixation was achieved using a long fluted intramedullary nail. The average follow-up time and time to union were 3 years (range, 0.25 to 9 years) and 13 months (range, 6 to 28 months), respectively. Eleven patients had nononcologic complications related to the index surgical procedure, including two patients with allograft nonunion. There were no infections. Three patients had amputations for local recurrence of their tumor. Twenty patients (80%) had no evidence of tumor at the time of follow-up. According to the Evaluation System of the Musculoskeletal Tumor Society, 80% of patients had a satisfactory result. No patient had a nononcologic complication resulting in total failure or amputation. The procedure of resection-arthrodesis of the knee using a large allograft with a long intramedullary nail provides patients with a stable, durable biological reconstruction that allows early weight-bearing, and the procedure carries a low incidence of infection.


Subject(s)
Arthrodesis/methods , Bone Nails , Bone Neoplasms/surgery , Fracture Fixation, Intramedullary/methods , Knee Joint/surgery , Neoplasms, Connective Tissue/surgery , Adolescent , Adult , Aged , Bone Transplantation/methods , Child , Female , Follow-Up Studies , Graft Survival , Humans , Male , Middle Aged , Postoperative Complications , Transplantation, Homologous/methods , Treatment Outcome
12.
J Orthop Res ; 11(2): 240-9, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8483036

ABSTRACT

Allograft transplantation with concomitant chemotherapy has proven successful in the treatment of malignant bone tumors. However, these chemotherapeutic agents may delay tissue healing, resulting in clinical complications. To clarify the effects of cisplatin on the healing of bone grafts, we studied the incorporation of stably fixed massive diaphyseal femoral syngeneic and allogeneic grafts in rats treated with cisplatin. These data were compared with those of historical controls from animals that did not receive cisplatin. Rats that were to receive a fresh syngeneic graft or frozen allogeneic graft were given cisplatin every 4 weeks starting 9 weeks preoperatively and continuing until the time of death. The total bone area of the graft in animals that received cisplatin was smaller than that of the graft in untreated control rats that did not receive cisplatin. The area of the frozen allograft did not increase between 2 and 4 months. Revascularization was incomplete in cisplatin-treated groups at 2 months, but by 4 months, vessel ingrowth in fresh syngeneic grafts approached control values. Frozen allografts remained poorly revascularized at 4 months. Host-graft union was poor at 2 months in cisplatin-treated rats compared with controls. In cisplatin-treated rats, the host-graft union of the frozen allograft remained inferior at 4 months while that of the syngeneic graft improved. Allogeneic cortical bone grafts are incorporated more slowly and incompletely than syngeneic grafts, and this handicap is exacerbated by the administration of cisplatin.


Subject(s)
Bone Development/drug effects , Bone Neoplasms/drug therapy , Bone Transplantation , Cisplatin/adverse effects , Host vs Graft Reaction/drug effects , Animals , Bone Neoplasms/surgery , Cisplatin/pharmacology , Combined Modality Therapy , Disease Models, Animal , Male , Postoperative Complications , Rats , Rats, Inbred Lew , Transplantation, Homologous , Transplantation, Isogeneic , Weight Loss/drug effects
13.
J Pediatr Orthop ; 12(6): 746-50, 1992.
Article in English | MEDLINE | ID: mdl-1452744

ABSTRACT

Seventeen children aged newborn to 14 years underwent major through-bone amputations or revision at our two institutions. Ten patients (group 1) had primary autogenous epiphyseal transplants taken from the amputated limb and used to cap the open medullary canal of the residual limb. Seven patients (group 2) did not have epiphyseal transplants. Nine of 10 patients in group 1 (90%) had no problems related to bone overgrowth or delay in prosthetic fitting. In group 2, six of seven patients (86%) had clinically symptomatic bony overgrowth of 20 months after the index amputation on the average. Four patients had surgical revisions. Therefore, provided healthy autogenous donor epiphyses are available, we recommend primary epiphyseal transplants to avoid the complications of bone overgrowth in childhood through-bone amputations.


Subject(s)
Amputation, Surgical/methods , Epiphyses/transplantation , Hyperostosis/prevention & control , Adolescent , Amputation, Surgical/adverse effects , Child , Child, Preschool , Female , Humans , Hyperostosis/etiology , Infant , Male , Reoperation , Retrospective Studies
14.
Hum Pathol ; 23(7): 729-35, 1992 Jul.
Article in English | MEDLINE | ID: mdl-1319390

ABSTRACT

The DNA content and proliferative indexes of seven cases of tenosynovial giant cell tumor of tendon sheath, diffuse type (TGCT-D); 11 cases of tenosynovial giant cell tumor of tendon sheath, localized type (TGCT-L); and seven cases of pigmented villonodular synovitis (PVNS) were analyzed by flow cytometry in an attempt to assess objectively their biologic differences. Three cases of TGCT-D manifested an aneuploid DNA content and four had a diploid DNA pattern. All cases of TGCT-L and PVNS showed a diploid DNA content. The proliferative indexes for TGCT-D were significantly higher than those found in the other two groups. There was no histopathologic feature that correlated with the aneuploid DNA pattern found in two of the three cases of TGCT-D. Only one of the three aneuploid DNA content TGCT-D cases displayed marked cellular pleomorphism with dense fibrous stroma; in that case there was recurrence 4 years after initial excision. Our data further support that TGCT-D, TGCT-L, and PVNS are histopathologically similar but clinically distinct lesions. The high proliferative indexes of TGCT-D may reflect a rapid, uncontrolled growth that may explain its aggressive biologic behavior. The presence of an aneuploid DNA pattern in some cases of TGCT-D in this study, coupled with the reported chromosomal abnormalities and occurrence of malignant transformation in these lesions, clearly supports their neoplastic nature.


Subject(s)
DNA, Neoplasm/analysis , Sarcoma, Synovial/genetics , Sarcoma, Synovial/pathology , Synovitis, Pigmented Villonodular/genetics , Synovitis, Pigmented Villonodular/pathology , Adult , Aged , Cell Division , Child , DNA/analysis , Female , Flow Cytometry , Humans , Male
15.
Skeletal Radiol ; 21(7): 466-9, 1992.
Article in English | MEDLINE | ID: mdl-1439900

ABSTRACT

This 50-year-old woman presented with progressive pain in the left thigh. Radiographs showed a 9 x 6 cm soft-tissue mass located at the lateral border of the left femur. Magnetic resonance (MR) examination showed an eccentric, nonhomogeneous, soft-tissue mass abutting the femur. The preoperative differential diagnosis was schwannoma, low-grade neurogenic tumor, large periosteal ganglion, or fibroma. At operation, the cut surface of the specimen had features of an organizing hematoma with recent remote hemorrhage and areas of fibrosis. Histopathological examination confirmed the presence of polarizable foreign body material in a background of foreign body reaction. The specimen represented a retained surgical sponge which had been present since the patient's surgery for a comminuted fracture 35 years earlier. Gossypiboma, or cotton balloma, is a term used to describe a mass within the body composed of cotton matrix. Radiopaque markers are now present on surgical sponges, and their appearances have been well documented. The gossypiboma, however, may still present a diagnostic problem if the marker is distorted by folding, twisting, or disintegration over a period of time. Without the radiopaque markers, retained sponges are difficult, if not impossible, to diagnose, as was the situation in this case.


Subject(s)
Bone Resorption/etiology , Femur/pathology , Foreign-Body Reaction/etiology , Hematoma/etiology , Surgical Sponges/adverse effects , Bone Resorption/pathology , Female , Foreign-Body Reaction/pathology , Hematoma/pathology , Humans , Magnetic Resonance Imaging , Middle Aged
16.
J Nucl Med ; 32(8): 1508-12, 1991 Aug.
Article in English | MEDLINE | ID: mdl-1869970

ABSTRACT

Twenty-five patients with mass lesions involving the musculoskeletal system were studied with positron emission tomography (PET) in order to determine if a relationship exists between histologic grade and tumor uptake of [fluorine-18]2-deoxy-2-fluoro-D-glucose (FDG). There were 6 benign lesions and 19 malignant lesions of various grades. A high correlation (Rho = 0.83) was found between the normalized uptake of tracer and the NCl grade. The high-grade malignancies had significantly greater (p = 0.0091) uptake of FDG than the combination of benign lesions and low-grade malignancies. All lesions with a normalized uptake value of 1.6 or greater were high-grade, while all lesions less than 1.6 represented either benign tumors or low grade malignancies. This strong relationship between FDG uptake and grade among neoplasms from a wide variety of cell types within a single organ system suggests that the technique may be useful in predicting grade even when the cell type is unknown.


Subject(s)
Bone Neoplasms/diagnostic imaging , Muscular Diseases/diagnostic imaging , Soft Tissue Neoplasms/diagnostic imaging , Tomography, Emission-Computed , Deoxyglucose/analogs & derivatives , Female , Fluorine Radioisotopes , Fluorodeoxyglucose F18 , Humans , Male , Middle Aged
18.
Gynecol Oncol ; 39(2): 108-14, 1990 Nov.
Article in English | MEDLINE | ID: mdl-2227582

ABSTRACT

Between 1948 and 1984, autopsies were performed on 305 patients with primary carcinomas of the cervix, endometrium, ovaries, fallopian tubes, vulva, and vagina. Skeletal metastases were detected premortem and at autopsy in 49 cases (16.1%): cervix, 20 (40.8%); endometrium, 17 (34.7%); ovary, 7 (14.3%); vulva, 4 (8.2%); fallopian tube, 1 (2%). There were no cases of osseous metastasis from vaginal carcinoma. The incidence and sites of metastasis from these gynecologic carcinomas were correlated with their clinical and histopathologic classifications. This clinicopathologic study, based on autopsy data, demonstrates that osseous metastases are not uncommon, are significantly greater than clinically appreciated, and correlate with advanced anatomic stage and histopathologic type and grade.


Subject(s)
Bone Neoplasms/secondary , Genital Neoplasms, Female/pathology , Autopsy , Bone Neoplasms/pathology , Fallopian Tube Neoplasms/pathology , Female , Follow-Up Studies , Humans , Neoplasm Staging , Ovarian Neoplasms/pathology , Uterine Cervical Neoplasms/pathology , Uterine Neoplasms/pathology , Vaginal Neoplasms/pathology , Vulvar Neoplasms/pathology
19.
J Comput Assist Tomogr ; 14(6): 960-2, 1990.
Article in English | MEDLINE | ID: mdl-2229575

ABSTRACT

Five patients with liposarcomas of the thigh were studied using positron emission tomography (PET) with [18F]2-deoxy-2-fluoroglucose (FDG). There were three low-grade tumors (all National Cancer Institute Grade 1 myxoid liposarcomas) and two high-grade tumors (both pleomorphic liposarcomas, Grades 2 and 3). The low-grade liposarcomas were easily identified with an average dose uptake ratio (DUR) of 1.38 +/- 0.045 (mean +/- SD). The high-grade lesions were more avid for FDG with a mean DUR of 2.45 +/- 0.24. There was a significant difference (p = 0.004) in the DUR for the two groups and the histological grade of malignancy was highly correlated with the DUR for FDG (Rho = 0.89). These findings suggest that FDG-PET may be useful for distinguishing between low-grade and high-grade liposarcomas.


Subject(s)
Deoxyglucose/analogs & derivatives , Liposarcoma/diagnostic imaging , Soft Tissue Neoplasms/diagnostic imaging , Tomography, Emission-Computed , Fluorodeoxyglucose F18 , Humans , Thigh
20.
J Hand Surg Am ; 15(4): 655-9, 1990 Jul.
Article in English | MEDLINE | ID: mdl-2199571

ABSTRACT

We report the clinicopathologic findings in two cases of chondrosarcoma of the small bones of the hand arising from a preexisting solitary enchondroma. A critical review of the previously reported 18 cases shows that only one is actually well-documented.


Subject(s)
Bone Neoplasms/pathology , Cartilage/pathology , Chondroma/pathology , Chondrosarcoma/pathology , Hand , Aged , Bone Neoplasms/surgery , Cell Transformation, Neoplastic/pathology , Chondroma/surgery , Chondrosarcoma/surgery , Female , Humans , Middle Aged
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