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Dive into the research topics where Paul C. McCormick is active.

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Featured researches published by Paul C. McCormick.


British Journal of Neurosurgery | 1989

Metastatic Carcinoma to the Pituitary Gland

Paul C. McCormick; Kalmon D. Post; Alexander d. Kandji; Arthur P. Hays

Four patients with metastatic carcinoma to the pituitary gland are presented. Two of these patients had no previous history of malignancy and, based on clinical, laboratory, and radiological evaluation, a preoperative diagnosis of pituitary adenoma was made. In one patient, the histological diagnosis of two consecutive tumour specimens, obtained 1 year apart, was pituitary adenoma. The correct diagnosis of metastatic renal-cell carcinoma was not ascertained until autopsy. In the second patient, a diffusely infiltrating breast carcinoma was diagnosed by mammography and confirmed by biopsy, after pathological examination of the sellar tumour revealed carcinoma. The third patient underwent mastectomy 3 years earlier for breast carcinoma and had known metastatic disease. The fourth patient had known metastatic endometrial carcinoma when she became symptomatic from a pituitary metastasis. The incidence, clinical features, and pathophysiology of metastatic carcinoma to the pituitary gland are discussed.


Neurosurgery | 2002

Spinal cord ependymoma: Radical surgical resection and outcome

Fadi Hanbali; Daryl R. Fourney; Eric Marmor; Dima Suki; Laurence D. Rhines; Jeffrey S. Weinberg; Ian E. McCutcheon; Ian Suk; Ziya L. Gokaslan; Ruth E. Bristol; Robert F. Spetzler; Harold L. Rekate; Michael J. Ebersold; Jacques Brotchi; Paul C. McCormick

OBJECTIVE Several authors have noted increased neurological deficits and worsening dysesthesia in the postoperative period in patients with spinal cord ependymoma. We describe the neurological progression and pain evolution of these patients over the 1-year period after surgery. In addition, our favored method of en bloc tumor resection is illustrated, and the rate of complications, recurrence, and survival in this group of patients is addressed. METHODS We operated on 26 patients (12 male and 14 female) with low-grade spinal cord ependymomas between 1975 and 2001. The median age at diagnosis was 42 years. Tumors extended into the cervical cord in 13 patients, the thoracic cord in 7 patients, and the conus medullaris in 6 patients. Eleven patients had previous surgery and/or radiation therapy. RESULTS We achieved a gross total resection in 88% of patients, whereas 8% had a subtotal resection and 4% had a biopsy. Only 1 patient developed a recurrence over a mean follow-up period of 31 months. CONCLUSION We conclude that radical surgical resection of spinal cord ependymomas can be safely achieved in the majority of patients. A trend toward neurological improvement from a postoperative deficit can be expected between 1 and 3 months after surgery and continues up to 1 year. Postoperative dysesthesias begin to improve within 1 month of surgery and are significantly better by 1 year after surgery. The best predictor of outcome is the preoperative neurological status.


Journal of Neuro-oncology | 2000

Intramedullary Ependymomas: Clinical Presentation, Surgical Treatment Strategies and Prognosis

Theodore H. Schwartz; Paul C. McCormick

Intramedullary ependymomas are rare tumors but comprise the majority of intramedullary glial neoplasms in the adult. These tumors are benign, slow-growing lesions which are optimally treated with gross-total surgical resection without adjuvant therapy. This objective can be attained safely in a majority, of patients. Post-operative functional outcome is related to pre-operative functional status. Hence, early diagnosis, prior to symptomatic progression, is critical to the successful treatment of these tumors. Adjuvant therapy is indicated for the rare malignant or disseminated tumor or following sub-total resection.


Surgical Neurology | 1996

Intramedullary spinal cord metastasis: Report of three cases and review of the literature

E. Sander Connolly; Christopher J. Winfree; Paul C. McCormick; Maureen Cruz; Bennett M. Stein

BACKGROUND Intramedullary spinal cord metastasis is rare; but it is being encountered with increasing frequency. Optimal treatment after diagnosis remains controversial. METHODS In the last 3 years, we have encountered three cases of intramedullary metastasis presenting as focal mass lesions with minimal systemic evidence of cancer. We present our results in these patients and review the literature in an effort to more optimally define both the natural course of this disease, as well as a potential subset of patients who might benefit from more aggressive treatment. RESULTS With the availability of more sensitive imaging techniques, these tumors are being diagnosed with increasing frequency. Magnetic resonance imaging is sensitive, but nonspecific, in distinguishing intramedullary spinal cord metastases from primary cord tumors. Urgent biopsy is often necessary prior to definitive treatment. Radiation with chemotherapy significantly prolongs survival. Radical subtotal resection may offer additional quality survival, especially in cases of metastatic melanoma with an occult primary. CONCLUSIONS Regardless of treatment, many patients survive less than 1 year. Intramedullary spinal cord metastasis is a devastating condition, but with appropriate diagnosis and aggressive treatment, selected patients may have substantially increased survival.


Neurosurgery | 1988

Cavernous malformations of the spinal cord.

Paul C. McCormick; Michelsen Wj; Kalmon D. Post; Carmel Pw; Bennett M. Stein

Six patients with intramedullary cavernous malformations of the spinal cord are presented. Four men and two women presented with acute, subacute, or episodic signs and symptoms of spinal cord dysfunction, ranging in duration from 3 days to 25 years. All patients underwent operative resection of the malformation. Complete removal was achieved in five patients. Neurological function either stabilized or improved postoperatively in all patients; follow-up ranged from 4 to 84 months. The increasing awareness of the propensity for recurrent hemorrhage, clinical features, and resectability of these malformations are discussed.


Neurosurgery | 1996

Surgical management of dumbbell and paraspinal tumors of the thoracic and lumbar spine.

Paul C. McCormick

The lateral extracavitary approach was used for single-staged tumor resection in 12 patients with complex dumbbell or paraspinal tumors of the thoracic and lumbar spine. Six women and six men (age, 28-72 yr) were treated between August 1990 and January 1994. The tumors included schwannoma (6 patients), malignant meningioma (1 patient), hemangioma (1 patient), chondrosarcoma (1 patient), osteocartilaginous exostosis (1 patient), radiation-induced osteogenic sarcoma (1 patient), and metastatic renal carcinoma (1 patient). Gross total resection was achieved in 11 patients. Radical subtotal removal was performed in the remaining patient, who had a malignant osteogenic sarcoma. Concomitant spinal stabilization with internal fixation and anterior interbody strut grafting was performed on two patients. No significant perioperative complications occurred. Ten patients were alive and clinically stable at follow-up visits ranging from 14 to 55 months. Two patients died from systemic tumor dissemination during the follow-up period. The lateral extracavitary approach is useful when extensive or difficult spinal and paraspinal exposure is required. The surgical aspects of these neoplasms and the technique of lateral extracavitary approach are described in detail.


Spine | 2003

National and Regional Rates and Variation of Cervical Discectomy With and Without Anterior Fusion, 1990-1999

Peter D. Angevine; Ray R. Arons; Paul C. McCormick

Study Design. A national hospitalization database was used to determine rates and trends in the treatment of cervical disc disease. Objective. To examine the temporal and geographic variations in hospitalizations and surgical procedures for cervical disc disease. Summary of Background Data. Studies of spinal surgery during the 1980s showed significant increases in the rates for all procedures, particularly those involving fusion. The management of cervical disc disease continues to be controversial. Methods. Data from the National Hospital Discharge Survey from 1990 through 1999 were analyzed. Records were selected and categorized according to an algorithm of International Classification of Diseases (ICD-9) procedure and diagnosis codes. Results. During the study period, the rate of hospitalization for surgical and nonsurgical treatment of cervical disc disease did not increase significantly. There was, however, a statistically significant increase in the proportion of hospitalizations for the surgical treatment of cervical disc disease that included a fusion procedure. There also was significant geographic variation in the rate of fusion procedures, with the South having the highest rate. Conclusions. Although the rate of surgery for cervical disc disease did not increase significantly during the 1990s, the rate of fusion procedures did rise significantly.


Neurosurgery | 1996

Surgical Management of Dumbbell Tumors of the Cervical Spine

Paul C. McCormick

Twelve patients with benign dumbbell tumors of the cervical spine were treated surgically between March 1991 and July 1994. Gross total resection was achieved in 11 patients, using a single-stage modified posterior midline exposure with laminectomy and complete unilateral facetectomy. This exposure provides contiguous intraspinal, foraminal, and extraforaminal access that extends up to 4 cm from the lateral dural margin. The surgical considerations of these tumors, including the surgical technique, potential spinal instability, vertebral artery, and risk of nerve root injury, are presented.


Journal of Neuro-oncology | 2004

Spinal Cord and Intradural-Extraparenchymal Spinal Tumors: Current Best Care Practices and Strategies

Andrew T. Parsa; Janet Lee; Ian F. Parney; Philip Weinstein; Paul C. McCormick; Christopher P. Ames

The management of patients with intradural spinal tumors differs in many respects from approaches taken for patients with intracranial tumors. Intramedullary lesions are often completely surrounded by normal spinal cord, displacing vital functional tracts eccentrically. Extramedullary lesions can drastically compress the spinal cord and nerve roots, reducing normal tissue to a ribbon-like consistency. The small amount of normal tissue relative to tumor has implications for surgery and postoperative adjuvant therapy. In addition, operative intervention must take spinal stability into consideration. In this report, we describe the current best care practices and strategies for patients with a diagnosis of spinal astrocytoma, ependymoma, hemangioblastoma, schwannoma, and meningioma. Treatment of patients with intradural tumors of the spinal cord and adjoining structures has changed over the past 20 years. Advances in many disciplines including neuroradiology, neurosurgery, neurooncology, and neuropathology have contributed to expediting diagnosis and improving outcomes.


Spine | 2009

Selecting treatment for patients with malignant epidural spinal cord compression-does age matter?: results from a randomized clinical trial.

John H. Chi; Ziya L. Gokaslan; Paul C. McCormick; Phillip A. Tibbs; Richard J. Kryscio; Roy A. Patchell

Study Design. Randomized clinical trial. Objective. To determine if age affects outcomes from differing treatments in patients with spinal metastases. Summary of Background Data. Recently, class I data were published supporting surgery with radiation over radiation alone for patients with malignant epidural spinal cord compression (MESCC). However, the criteria to properly select candidates for surgery remains controversial and few independent variables which predict success after treatment have been identified. Methods. Data for this study was obtained in a randomized clinical trial comparing surgery versus radiation for MESCC. Hazard ratios were determined for the effect of age and the interaction between age and treatment. Age estimates at which prespecified relative risks could be expected were calculated with greater than 95% confidence to suggest possible age cut points for further stratification. Multivariate models and Kaplan-Meier curves were tested using stratified cohorts for both treatment groups in the randomized trial each divided into 2 age groups. Results. Secondary data analysis with age stratification demonstrated a strong interaction between age and treatment (hazard ratio = 1.61, P = 0.01), such that as age increases, the chances of surgery being equal to radiation alone increases. The best estimate for the age at which surgery is no longer superior to radiation alone was calculated to be between 60 and 70 years of age (95% CI), using sequential prespecified relative risk ratios. Multivariate modeling and Kaplan-Meier curves for stratified treatment groups showed that there was no difference in outcome between treatments for patients ≥65 years of age. Ambulation preservation was significantly prolonged in patients <65 years of age undergoing surgery compared to radiation alone (P = 0.002). Conclusion. Age is an important variable in predicting preservation of ambulation and survival for patiens being treated for spinal metastases. Our results provide compelling evidence for the first time that particular age cut points may help in selecting patients for surgical or nonsurgical intervention based on outcome.

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Andrew T. Parsa

NewYork–Presbyterian Hospital

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Volker K. H. Sonntag

St. Joseph's Hospital and Medical Center

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