Sporadic unifocal infantile myofibromatosis involving the skull

1999 ◽  
Vol 90 (6) ◽  
pp. 1129-1132 ◽  
Author(s):  
Paul W. Detwiler ◽  
Randall W. Porter ◽  
Stephen W. Coons ◽  
Robert F. Spetzler ◽  
Carlos A. Carrion ◽  
...  

✓ Infantile myofibromatosis involving the skull is a benign disease if there is a solitary lesion. However, the multifocal form with skull involvement may portend a lethal course in the 1st year of life if there is involvement of the heart, lungs, or gastrointestinal tract. The authors report the case of a 3-year-old boy with an enlarging left parietal skull lesion that had been present since infancy. Increasing pain and the need to obtain tissue for diagnosis led to resection of the lesion by means of a small craniectomy. Further evaluation revealed no other lesions. A distinctly rare disease is presented, and the need for staging in children younger than 2 years of age is suggested to rule out cardiac, pulmonary, or gastrointestinal involvement.

1972 ◽  
Vol 37 (1) ◽  
pp. 27-29 ◽  
Author(s):  
Steven B. Karch

✓ Review of 2206 consecutive necropsies showed evidence of hemorrhagic ulceration of the upper gastrointestinal tract in 7.2%. The incidence in patients dying from intracranial disorders was found to be twice that of those dying from all other causes (12.5% vs 6.0%). The distribution of lesions within the two groups was also different in that esophageal ulceration was more common in the neurological group (p < .001), while duodenal ulcers were more common in the non-neurological group (p < .001).


1982 ◽  
Vol 56 (5) ◽  
pp. 722-727 ◽  
Author(s):  
Duncan B. Carpenter ◽  
W. Jost Michelsen ◽  
Arthur P. Hays

✓ Carcinoma of the choroid plexus is an extremely rare disease with a particularly virulent course. A case is reported in the left lateral ventricle of a young woman who is well 1 year after total excision of the tumor. The four previously reported patients with this disease who did well (two males and two females) were all children. Three of the four were treated with surgery followed by radiotherapy, and one with surgery alone. Although it appears possible that gross total removal may be curative, radiation therapy is suggested because of the distinct possibility that even the least aggressive-appearing lesions may degenerate and become rapidly fatal. Chemotherapy, although not used in any of the cases reported, is suggested as a possible adjunct in the treatment of this disease.


1979 ◽  
Vol 51 (1) ◽  
pp. 42-46 ◽  
Author(s):  
Saul Balagura ◽  
Andrew G. Frantz ◽  
Edgar M. Housepian ◽  
Peter W. Carmel

✓ Serum prolactin levels were determined in 205 patients with a variety of intracranial diseases, including 70 cases with pituitary tumors. It is concluded that although the absence of elevated prolactin levels does not help to rule out pituitary pathology, the presence of hyperprolactinemia is highly specific for diseases of the pituitary and hypothalamus, and prolactin determination should be part of the regular work-up of pituitary tumor suspects. Excluding known causes of hyperprolactinemia, such as tranquilizing drug ingestion, the presence of neurological disease outside the hypothalamic-pituitary area was not associated with increased serum prolactin concentrations.


1989 ◽  
Vol 71 (2) ◽  
pp. 290-292 ◽  
Author(s):  
C. F. Fung ◽  
Thomas H. K. Ng ◽  
W. T. Wong

✓ Sparganosis of the spinal cord is a rare disease: only two cases have previously been described. A third case of spinal sparganosis is reported in which a sparganum was removed from the central canal of the patient's spinal cord. The clinical presentation and pathology are described. A brief review of the life cycle of the Spirometra is given and the possible mode of infestation is discussed.


2001 ◽  
Vol 95 (5) ◽  
pp. 853-858 ◽  
Author(s):  
Giorgio Iaconetta ◽  
Enrico Tessitore ◽  
Madjid Samii

Object. The anatomy of the abducent nerve is well known; its duplication (ranging from 5 to 28.6%), however, has rarely been reported in the literature. The authors performed a microanatomical study in 100 cadaveric specimens (50 heads) to evaluate the prevalence of this phenomenon and to provide a clear anatomical description of the course and relationships of the nerve. The surgery-related implications of this rare anatomical variant will be highlighted. Methods. The 50 human cadaveric heads (100 specimens) were embalmed in a 10% formalin solution for 3 weeks. Fifteen of them were injected with colored neoprene latex. A duplicated abducent nerve was found in eight specimens (8%). In two (25%) of these eight specimens the nerve originated at the pontomedullary sulcus as two independent trunks: in one case the superior trunk was thicker than the inferior and in the other it was thinner. In the other six cases (75%) the nerve originated as a single trunk, splitting in two trunks into the cisternal segment: in two of them the trunks ran below the Gruber ligament, whereas in four specimens one trunk ran below and one above it. In all the specimens, the duplicated nerves fused again into the cavernous sinus, just after the posterior genu of the internal carotid artery. Conclusions. Although the presence of a duplicated abducent nerve is a rare finding, preoperative magnetic resonance imaging should be performed to rule out this possibility, thus tailoring the operation to avoid postoperative deficits.


1987 ◽  
Vol 67 (6) ◽  
pp. 931-934 ◽  
Author(s):  
Sze-Tong Chan ◽  
C. H. Tse ◽  
Y. S. Chan ◽  
Dawson Fong

✓ Cerebral sparganosis is a rare disease; to date only eight cases have been described. Two new cases of cerebral sparganosis occurring in Chinese patients living in a metropolitan area are reported. Their clinical presentation and investigative results are presented and the operative and histological findings detailed. A brief review of the condition is given and the possible source of infection discussed.


1977 ◽  
Vol 47 (4) ◽  
pp. 609-612 ◽  
Author(s):  
Richard W. Leech ◽  
Lee A. Christoferson ◽  
Roger L. Gilbertson

✓ A case of dysplastic gangliocytoma, or Lhermitte-Duclos disease, of the cerebellum is reported. The patient was the seventh reported survivor of this rare disease. A review of the known biology of the disease allows some optimism. The treatment of choice appears to be surgical resection only.


1995 ◽  
Vol 82 (3) ◽  
pp. 489-492 ◽  
Author(s):  
Michael D. Partington ◽  
Bernd W. Scheithauer ◽  
David G. Piepgras

✓ An elevated serum carcinoembryonic antigen (CEA) without evidence of neoplasia was noted in an 84-year-old woman. She subsequently developed a lytic skull lesion, which at surgery proved to be an atypical meningioma. Immunohistochemical analysis demonstrated that this tumor was producing CEA. This aggressive meningioma required two further resections and adjuvant radiotherapy in the following 18 months. Serum elevation of CEA has been reported only twice in association with meningiomas; both of those tumors were of the secretory subtype.


2000 ◽  
Vol 93 (2) ◽  
pp. 309-311
Author(s):  
Anupam Jindal ◽  
Somil Kansal ◽  
Ashok Kumar Mahapatra

✓ The authors describe the case of a 3-year-old girl who presented with a dorsal split cord malformation (SCM) and was found to have eventration of the diaphragm. Although the child did not undergo surgery for eventration, its presence suggests a need for careful preoperative planning and clinical evaluation to rule out or confirm the anomalies associated with spinal dysraphism or SCM.


1995 ◽  
Vol 83 (2) ◽  
pp. 222-224 ◽  
Author(s):  
William C. Olivero ◽  
J. Richard Lister ◽  
Patrick W. Elwood

✓ Little is known about the natural history and growth rate of asymptomatic meningiomas. To better delineate this problem, the authors reviewed the clinical records and imaging studies of the last 60 patients diagnosed with asymptomatic meningiomas at their institution. There were 45 women and 15 men, whose ages ranged from 38 to 84 years, with a mean age of 66 years. The most common tumor location was convexity (25 patients), but virtually all locations were represented. Three patients were lost to follow up. The average clinical follow-up review of the remaining 57 patients was 32 months (range 6 months to 15 years). None of the patients became symptomatic from an enlarging tumor during their follow-up period. Typically, once a meningioma was diagnosed, follow-up scans were obtained at 3 months, 9 months, and then yearly or every other year thereafter. Forty-five patients underwent follow-up scans, with comparison of tumor size to that found on the initial scan, over a period ranging from 3 months to 15 years. Thirty-five patients have shown no growth in their tumor size, with an average imaging follow up of 29 months (range 3–72 months). Ten patients have shown tumor growth calculated as an increase in the maximum diameter of the tumor. This growth ranged from 0.2 cm over 180 months to 1 cm over 12 months, with an average of 0.24 cm per year. Average imaging follow up for these patients was 47 months (range 6 months to 15 years). The authors conclude that patients with asymptomatic meningiomas need close clinical and radiological follow up to rule out other disease processes and to rule out rapidly enlarging tumors. Although the average follow-up time was short, the vast majority of these tumors appeared to show minimal or no growth over periods of time measured in years. With modern noninvasive imaging techniques, these tumors can be safely observed until they enlarge significantly or become symptomatic.


Sign in / Sign up

Export Citation Format

Share Document