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1
benign neoplasm of joint 2005:2010[pubdate] *count=100
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Items 1 to 85 of about 85
1.
Cao Y, Paner GP, Perry KT, Flanigan RC, Campbell SC, Picken MM:
Renal neoplasms in younger adults: analysis of 112 tumors from a single institution according to the new 2004 World Health Organization classification and 2002 American Joint Committee on Cancer Staging System.
Arch Pathol Lab Med
; 2005 Apr;129(4):487-91
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[Title]
Renal neoplasms in younger adults: analysis of 112 tumors from a single institution according to the new 2004 World Health Organization classification and 2002 American
Joint
Committee on Cancer Staging System.
Recent modification of the World Health Organization histologic classification and the American
Joint
Committee on Cancer staging system of adult renal tumors further highlighted the need for case analysis in this age group.
The tumors were reevaluated according to the 2004 World Health Organization classification and the 2002 American
Joint
Committee on Cancer staging system.
Seventeen percent of these tumors had multilocular cystic features involving more than 50% of the
tumor
volume (55%-85%).
The number of oncocytomas was also significantly lower in younger adults than in older adults (2% vs 11%, P < .001), and this presumably age-related
benign neoplasm
was not identified in patients younger than 40 years in this study.
In contrast, the miscellaneous
tumor
category showed a remarkable increase, from 4% in older adults to 26% in younger adults (P < .001).
Younger female adults tended to have more
benign
miscellaneous neoplasms than did their male counterparts (64% vs 36%, P < .001).
Malignant and
benign
renal neoplasms tend to have a contrasting sex distribution in younger adults.
[MeSH-minor]
Adult. Age Distribution. Female. Humans. Male.
Neoplasm
Staging. Sex Distribution
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(PMID = 15794671.001).
[ISSN]
1543-2165
[Journal-full-title]
Archives of pathology & laboratory medicine
[ISO-abbreviation]
Arch. Pathol. Lab. Med.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
2.
Unglaub F, Loos B, Wolf MB, Dragu A, Amann K, Horch RE:
Malignant Natural-Killer cell neoplasm presenting as a mucous cyst on the distal interphalangeal joint of the finger.
Arch Orthop Trauma Surg
; 2009 Dec;129(12):1613-6
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[Title]
Malignant Natural-Killer cell
neoplasm
presenting as a mucous cyst on the distal interphalangeal
joint of
the finger.
The analysis revealed the presence of a Natural-Killer cell
neoplasm
.
This case illustrates and stresses the importance of a pathohistological examination when doubts arise about the initial
diagnosis
of a
benign
tumorous lesion.
[MeSH-minor]
Aged. Cysts /
diagnosis
. Fingers. Humans. Male
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(PMID = 19084980.001).
[ISSN]
1434-3916
[Journal-full-title]
Archives of orthopaedic and trauma surgery
[ISO-abbreviation]
Arch Orthop Trauma Surg
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
Germany
3.
Maceroli M, Uglialoro AD, Beebe KS, Benevenia J:
Recurrent knee pain in an athletic adult: multiple schwannomas secondary to schwannomatosis: a case report.
Am J Orthop (Belle Mead NJ)
; 2010 Nov;39(11):E119-22
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In our case, a 28-year-old athletic man underwent a right knee excisional biopsy for multifocal,
benign
schwannomatosis.
Excisional biopsy of discrete masses was performed and histologic examination revealed recurrent
benign
schwannomatosis.
To our knowledge, this is the second reported case of recurrent
benign
schwannomatosis.
[MeSH-major]
Athletes.
Neoplasm
Recurrence, Local. Neurilemmoma /
diagnosis
. Neurofibromatoses /
diagnosis
. Pain /
diagnosis
. Peripheral Nervous System Neoplasms /
diagnosis
. Skin Neoplasms /
diagnosis
[MeSH-minor]
Adult. Biomarkers,
Tumor
/ metabolism. Humans. Ilium / pathology. Ilium / surgery. Knee
Joint
/ pathology. Knee
Joint
/ physiopathology. Knee
Joint
/ surgery. Male. Tomography, X-Ray Computed. Treatment Outcome
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(PMID = 21623424.001).
[ISSN]
1934-3418
[Journal-full-title]
American journal of orthopedics (Belle Mead, N.J.)
[ISO-abbreviation]
Am J. Orthop.
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Review
[Publication-country]
United States
[Chemical-registry-number]
0 / Biomarkers, Tumor; Schwannomatosis
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4.
Bahamonde L, Catalan J:
Bone tumors around the knee: risks and benefits of arthroscopic procedures.
Arthroscopy
; 2006 May;22(5):558-64
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Although most primary bone tumors and soft tissue tumors arise around the knee
joint
, many patients with tumoral conditions attribute their symptoms to traumatic events.
Arthroscopy is the preferred method for
diagnosis
and treatment of knee
joint
disease, but even a minimally invasive procedure may have adverse consequences in the presence of an unsuspected
neoplasm
.
In addition, arthroscopy is a useful adjunct during surgical treatment of patients with certain juxta-articular
benign
bone tumors.
In this Current Concepts review, we consider the risks and benefits of arthroscopy in the presence of tumors about the knee
joint
.
[MeSH-major]
Arthroscopy. Bone Neoplasms / surgery. Knee
Joint
[MeSH-minor]
Biopsy. Humans. Soft Tissue Neoplasms /
diagnosis
. Soft Tissue Neoplasms / surgery
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(PMID = 16651168.001).
[ISSN]
1526-3231
[Journal-full-title]
Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association
[ISO-abbreviation]
Arthroscopy
[Language]
eng
[Publication-type]
Journal Article; Review
[Publication-country]
United States
[Number-of-references]
29
5.
Boriani S, Bandiera S, Donthineni R, Amendola L, Cappuccio M, De Iure F, Gasbarrini A:
Morbidity of en bloc resections in the spine.
Eur Spine J
; 2010 Feb;19(2):231-41
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The study was set up to correlate
diagnosis
, staging and treatment with the outcome.
Oncological and functional results were recorded for all patients at periodic,
diagnosis
-related controls, until death or the latest follow-up examination (from 0 to 211 months, median 47 months, 25th-75th percentile 22-85 months).
Of the 35 patients with a recurrent or contaminated
tumor
, 16 (45.7%) suffered at least one complication; by contrast, complications arose in 31 (31.3%) of the 99 patients who had had no previous treatment and who underwent the whole of their treatment in the same center (P = 0.125).
Re-operations were mostly due to
tumor
recurrences, but also to hardware failures, wound dehiscence, hematomas and aortic dissection.
En bloc resection is able to improve the prognosis of aggressive
benign
and low-grade malignant tumors in the spine; however, complications are not rare and possibly fatal.
[MeSH-minor]
Adult. Aged. Aortic Rupture / mortality. Equipment Failure. Female. Humans. Male. Middle Aged. Mortality.
Neoplasm
Recurrence, Local / mortality.
Neoplasm
Recurrence, Local / pathology.
Neoplasm
Recurrence, Local / surgery. Outcome Assessment (Health Care). Radiotherapy / adverse effects. Reoperation / mortality. Retrospective Studies. Surgical Wound Dehiscence / mortality. Surgical Wound Infection / mortality. Treatment Outcome
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[Cites]
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[ISSN]
1432-0932
[Journal-full-title]
European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
[ISO-abbreviation]
Eur Spine J
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
[Other-IDs]
NLM/ PMC2899819
6.
Singh S, Singh R, Singh UP, Rai SN, Novakovic KR, Chung LW, Didier PJ, Grizzle WE, Lillard JW Jr:
Clinical and biological significance of CXCR5 expressed by prostate cancer specimens and cell lines.
Int J Cancer
; 2009 Nov 15;125(10):2288-95
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While prostate
tumor
tissues with Gleason scores >or= 7, displayed predominantly nuclear CXCR5 expression patterns, PCa specimens with Gleason scores <or= 6 showed predominantly membrane and cytoplasmic expression patterns that were comparable to
benign
prostatic hyperplasia (BPH).
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[Cites]
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[ISSN]
1097-0215
[Journal-full-title]
International journal of cancer
[ISO-abbreviation]
Int. J. Cancer
[Language]
ENG
[Grant]
United States / NCI NIH HHS / CA / U54 CA118638; United States / NCRR NIH HHS / RR / G12 RR003034; United States / NCI NIH HHS / CA / U54 CA118623; United States / NCI NIH HHS / CA / U54 CA118948; United States / NIMHD NIH HHS / MD / P60 MD000525-03; United States / NIMHD NIH HHS / MD / MD00525; United States / NIMHD NIH HHS / MD / P60 MD000525; United States / NIAID NIH HHS / AI / AI057808; United States / NCI NIH HHS / CA / U54 CA118638-06; United States / NIGMS NIH HHS / GM / S06 GM008248; United States / NIGMS NIH HHS / GM / GM09248; United States / NIAID NIH HHS / AI / R01 AI057808; United States / NIDDK NIH HHS / DK / DK58967; United States / NIAID NIH HHS / AI / AI057808-05; United States / NCI NIH HHS / CA / U54 CA118638-07; United States / NCI NIH HHS / CA / U24 CA086359; United States / NIGMS NIH HHS / GM / GM08248; United States / NCI NIH HHS / CA / U56 CA092078; United States / NIAID NIH HHS / AI / R01 AI057808-05; United States / NCI NIH HHS / CA / CA086359; United States / NCI NIH HHS / CA / CA092078
[Publication-type]
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
United States
[Chemical-registry-number]
0 / CXCL13 protein, human; 0 / CXCR5 protein, human; 0 / Chemokine CXCL13; 0 / RNA, Messenger; 0 / Receptors, CXCR5; EC 3.4.24.- / Matrix Metalloproteinases
[Other-IDs]
NLM/ NIHMS137666; NLM/ PMC3600527
7.
Singh S, Singh R, Sharma PK, Singh UP, Rai SN, Chung LW, Cooper CR, Novakovic KR, Grizzle WE, Lillard JW Jr:
Serum CXCL13 positively correlates with prostatic disease, prostate-specific antigen and mediates prostate cancer cell invasion, integrin clustering and cell adhesion.
Cancer Lett
; 2009 Sep 28;283(1):29-35
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In this study, we present the first evidence that CXCL13, the only ligand for CXCR5, and IL-6 were significantly elevated in PCa patient serum compared to serum from subjects with
benign
prostatic hyperplasia (BPH), or high-grade prostatic intraepithelial neoplasia (HGPIN) as well as normal healthy donors (NHD).
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[ISSN]
1872-7980
[Journal-full-title]
Cancer letters
[ISO-abbreviation]
Cancer Lett.
[Language]
ENG
[Grant]
United States / NCRR NIH HHS / RR / G12 RR003034-27; United States / NCRR NIH HHS / RR / G12 RR003034-23; United States / NCRR NIH HHS / RR / G12 RR003034; United States / NCI NIH HHS / CA / U24 CA086359-10; United States / NIMHD NIH HHS / MD / P60 MD000525-03; United States / NIMHD NIH HHS / MD / MD00525; United States / NIMHD NIH HHS / MD / P60 MD000525; United States / NIAID NIH HHS / AI / AI057808; United States / NCRR NIH HHS / RR / RR003034-23; United States / NIGMS NIH HHS / GM / S06 GM008248; United States / NIGMS NIH HHS / GM / GM09248; United States / NCRR NIH HHS / RR / RR03034; United States / NIGMS NIH HHS / GM / GM008248-22; United States / NIAID NIH HHS / AI / R01 AI057808; United States / NIDDK NIH HHS / DK / DK58967; United States / NCI NIH HHS / CA / U24CA86359.; United States / NCI NIH HHS / CA / U24 CA086359; United States / NIGMS NIH HHS / GM / GM08248; United States / NIGMS NIH HHS / GM / S06 GM008248-22; United States / NCI NIH HHS / CA / U56 CA092078; United States / NCI NIH HHS / CA / CA086359-10; United States / NCI NIH HHS / CA / CA092078
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
Ireland
[Chemical-registry-number]
0 / Biomarkers, Tumor; 0 / CXCL13 protein, human; 0 / CXCR5 protein, human; 0 / Chemokine CXCL13; 0 / Integrins; 0 / Interleukin-6; 0 / Receptors, CXCR5; EC 3.4.21.77 / Prostate-Specific Antigen
[Other-IDs]
NLM/ NIHMS140687; NLM/ PMC3600557
8.
Eversole R, Su L, ElMofty S:
Benign fibro-osseous lesions of the craniofacial complex. A review.
Head Neck Pathol
; 2008 Sep;2(3):177-202
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[Title]
Benign
fibro-osseous lesions of the craniofacial complex. A review.
Benign
fibro-osseous lesions of the craniofacial complex are represented by a variety of disease processes that are characterized by pathologic ossifications and calcifications in association with a hypercellular fibroblastic marrow element.
The definitive
diagnosis
can rarely be rendered on the basis of histopathologic features alone; rather, procurement of a final
diagnosis
is usually dependent upon assessment of microscopic, clinical and imaging features together.
[MeSH-major]
Cementoma /
diagnosis
. Fibroma, Ossifying /
diagnosis
. Fibrous Dysplasia of Bone /
diagnosis
. Osteitis Deformans /
diagnosis
. Skull Neoplasms /
diagnosis
[MeSH-minor]
DNA,
Neoplasm
/ analysis. Humans. Mutation
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(PMID = 20614314.001).
[ISSN]
1936-0568
[Journal-full-title]
Head and neck pathology
[ISO-abbreviation]
Head Neck Pathol
[Language]
eng
[Publication-type]
Journal Article; Review
[Publication-country]
United States
[Chemical-registry-number]
0 / DNA, Neoplasm
[Other-IDs]
NLM/ PMC2807558
[Keywords]
NOTNLM ; Benign fibroosseous lesions / Cementoma / Cementoosseous dysplasia / Fibrous dysplasia / Ossifying fibroma / Osteitis deformans
9.
Kalish LH, Ng T, Kalnins I, Da Cruz MJ:
Pseudogout mimicking an infratemporal fossa tumor.
Head Neck
; 2010 Jan;32(1):127-32
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[Title]
Pseudogout mimicking an infratemporal fossa
tumor
.
METHODS AND RESULTS: We present a case of a 71-year-old woman who presented with worsening facial pain, trismus, and a large mass in her infratemporal fossa with minimal associated temporomandibular
joint
destruction.
CONCLUSION: The clinical and radiological features of patients with tophaceous pseudogout frequently mimic those of a
benign
or malignant
neoplasm of
the infratemporal fossa, often resulting in more radical surgery.
[MeSH-major]
Chondrocalcinosis /
diagnosis
. Chondrocalcinosis / surgery. Skull Base Neoplasms /
diagnosis
. Skull Base Neoplasms / surgery. Temporal Bone / surgery
[MeSH-minor]
Aged.
Diagnosis
, Differential. Facial Pain / etiology. Female. Humans. Otorhinolaryngologic Surgical Procedures / methods. Temporomandibular
Joint
/ pathology. Treatment Outcome. Trismus / etiology
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(PMID = 19283846.001).
[ISSN]
1097-0347
[Journal-full-title]
Head & neck
[ISO-abbreviation]
Head Neck
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
10.
Carlson JA, Ross JS, Slominski AJ:
New techniques in dermatopathology that help to diagnose and prognosticate melanoma.
Clin Dermatol
; 2009 Jan-Feb;27(1):75-102
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Routine light microscopy supplemented with immunohistochemistry in cases of metastatic or spindle cell melanoma are standards of care for the
diagnosis
and staging of melanoma.
Not all melanocytic tumors can be confidently classified as melanoma or
benign
nevus by histology, however.
In addition,
tumor
thickness and ulceration, the current American
Joint
Classification on Cancer prognosticators for primary cutaneous (stages I and II) melanoma used in clinical practice, do not perfectly predict an individual's clinical course.
Recent advances in molecular techniques and bioinformatics mandate testing and use of novel methods for the detection,
diagnosis
, and classification of melanocytic tumors that can accurately predict
tumor
behavior and help in selecting the most optimal and individualized therapy.
[MeSH-minor]
Cytogenetic Analysis. Dermatology / methods. Humans. Immunohistochemistry. Molecular Diagnostic Techniques.
Neoplasm
Staging. Prognosis
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(PMID = 19095155.001).
[ISSN]
1879-1131
[Journal-full-title]
Clinics in dermatology
[ISO-abbreviation]
Clin. Dermatol.
[Language]
eng
[Publication-type]
Journal Article; Review
[Publication-country]
United States
[Number-of-references]
288
11.
Suresh S, Saifuddin A:
Unveiling the 'unique bone': a study of the distribution of focal clavicular lesions.
Skeletal Radiol
; 2008 Aug;37(8):749-56
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There is no study discussing the differential
diagnosis
of clavicular lesions based on the site of occurrence or age at presentation.
This study aims to determine whether the distribution of lesions affecting the clavicle and age at presentation aid in the differential
diagnosis
of focal clavicular lesions.
Virtually, all patients had been referred as suspected
neoplasm
.
Patients <20 years (n = 27) had non-neoplastic or
benign
lesions.
The lesions most commonly affected the medial third (n = 35) and were predominantly non-neoplastic or
benign
.
The middle third was affected in 15 patients and showed both
benign
and malignant lesions.
CONCLUSIONS: The clavicle is not a primary common site for any particular tumour; hence,
diagnosis
of the lesions can be challenging.
Our study has suggested that few factors like age and site of the lesions may be helpful in
diagnosis
.
[MeSH-major]
Bone Diseases /
diagnosis
. Clavicle / pathology
[MeSH-minor]
Adult. Biopsy. Bone Neoplasms /
diagnosis
.
Diagnosis
, Differential. Female. Humans. Magnetic Resonance Imaging / methods. Male. Middle Aged. Osteomyelitis /
diagnosis
. Tomography, X-Ray Computed / methods
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[ISSN]
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[Journal-full-title]
Skeletal radiology
[ISO-abbreviation]
Skeletal Radiol.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
12.
Lee JW, Kim BS, Lee DS, Chung JK, Lee MC, Kim S, Kang WJ:
18F-FDG PET/CT in mediastinal lymph node staging of non-small-cell lung cancer in a tuberculosis-endemic country: consideration of lymph node calcification and distribution pattern to improve specificity.
Eur J Nucl Med Mol Imaging
; 2009 Nov;36(11):1794-802
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Mediastinal node staging was determined using the American
Joint
Committee on Cancer (AJCC) staging system.
After lymph nodes with calcification and bilateral hilar distribution were considered
benign
, sensitivity and specificity of PET/CT were 75% and 89% on a per-patient basis and 66% and 96% on a per-node station basis.
[MeSH-minor]
Contrast Media. Endemic Diseases. False Positive Reactions. Female. Humans. Male. Middle Aged.
Neoplasm
Staging. Positron-Emission Tomography. Radiography, Thoracic. Sensitivity and Specificity. Tomography, X-Ray Computed
Genetic Alliance.
consumer health - Lung Cancer
.
Genetic Alliance.
consumer health - Non-small cell lung cancer
.
Genetic Alliance.
consumer health - Tuberculosis
.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
MedlinePlus Health Information.
consumer health - Tuberculosis
.
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]
[Cites]
Chest. 1997 Jun;111(6):1718-23
[
9187199.001
]
(PMID = 19430783.001).
[ISSN]
1619-7089
[Journal-full-title]
European journal of nuclear medicine and molecular imaging
[ISO-abbreviation]
Eur. J. Nucl. Med. Mol. Imaging
[Language]
eng
[Publication-type]
Clinical Trial; Journal Article
[Publication-country]
Germany
[Chemical-registry-number]
0 / Contrast Media; 0Z5B2CJX4D / Fluorodeoxyglucose F18
13.
Mackenzie H, Gulati V, Tross S:
A rare case of a swollen knee due to disseminated synovial chondromatosis: a case report.
J Med Case Rep
; 2010;4:113
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INTRODUCTION: A synovial chondromatosis is a rare
benign neoplasm
on the synovium.
Although described as a
benign
disease, it can be very destructive and can cause severe osteoarthritis and pain.
To the best of our knowledge, we report the first known case of an extensive presentation of this intra-articular and extra-articular disease of the knee
joint
.
CONCLUSIONS: Although synovial chondromatosis is described as a
benign
disease, it can be very destructive and debilitating.
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[Cites]
J Arthroplasty. 2008 Apr;23(3):395-400
[
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]
[Cites]
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[
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]
[Cites]
J Bone Joint Surg Am. 2007 Jun;89(6):1321-8
[
17545437.001
]
(PMID = 20416049.001).
[ISSN]
1752-1947
[Journal-full-title]
Journal of medical case reports
[ISO-abbreviation]
J Med Case Rep
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
[Other-IDs]
NLM/ PMC2873448
14.
Mentzel T, Toennissen J, Rütten A, Schaller J:
Palmar atypical lipomatous tumour with spindle cell features (well-differentiated spindle cell liposarcoma): a rare neoplasm arising in an unusual anatomical location.
Virchows Arch
; 2005 Mar;446(3):300-4
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[Title]
Palmar atypical lipomatous tumour with spindle cell features (well-differentiated spindle cell liposarcoma): a rare
neoplasm
arising in an unusual anatomical location.
Lipomatous tumours, both
benign
and malignant, arising on the hands are uncommon.
The
neoplasm
presented as a long-standing, exophytic
neoplasm
measuring 9 x 9 cm.
The well-circumscribed
neoplasm
was completely excised, and margins were tumour free.
Histologically, the
neoplasm
showed features closely resembling spindle cell lipoma, being composed of mature adipocytic cells associated with bland, neuroid spindle cells staining positively for CD34.
Aypical lipomatous tumour with spindle cell features may arise very rarely in palmar location and has to be distinguished from a number
of benign
and malignant mesenchymal neoplasms.
[MeSH-minor]
Diagnosis
, Differential. Humans. Immunohistochemistry. Male. Middle Aged
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[Cites]
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[
14299665.001
]
(PMID = 15719245.001).
[ISSN]
0945-6317
[Journal-full-title]
Virchows Archiv : an international journal of pathology
[ISO-abbreviation]
Virchows Arch.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
15.
Zhang Q, Zhao H, Maheshwari AV, Cai L, Yu F, Niu X:
Isolated cardiac metastasis from a histologically "benign" giant-cell tumor of the distal end of the femur: a case report.
J Bone Joint Surg Am
; 2010 Nov 17;92(16):2725-31
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[Title]
Isolated cardiac metastasis from a histologically "
benign
" giant-cell
tumor
of the distal end of the femur: a case report.
[MeSH-major]
Bone Neoplasms / pathology. Femur / pathology. Giant Cell
Tumor
of Bone / secondary. Heart Neoplasms / secondary
[MeSH-minor]
Adult. Biopsy, Needle. Disease Progression. Fatal Outcome. Heart Failure /
diagnosis
. Humans. Immunohistochemistry. Male.
Neoplasm
Staging. Orthopedic Procedures / methods. Tomography, X-Ray Computed / methods
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(PMID = 21084583.001).
[ISSN]
1535-1386
[Journal-full-title]
The Journal of bone and joint surgery. American volume
[ISO-abbreviation]
J Bone Joint Surg Am
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
16.
Kim J, Takeuchi H, Lam ST, Turner RR, Wang HJ, Kuo C, Foshag L, Bilchik AJ, Hoon DS:
Chemokine receptor CXCR4 expression in colorectal cancer patients increases the risk for recurrence and for poor survival.
J Clin Oncol
; 2005 Apr 20;23(12):2744-53
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METHODS: CRC cell lines (n = 6) and
tumor
specimens (n = 139) from patients with different American
Joint
Committee on Cancer (AJCC) stages of CRC were assessed.
CXCR4 expression in
tumor
and
benign
specimens was assessed by quantitative real-time reverse transcription polymerase chain reaction and correlated with disease recurrence and overall survival.
RESULTS: High CXCR4 expression in
tumor
specimens (n = 57) from AJCC stage I/II patients was associated with increased risk for local recurrence and/or distant metastasis (risk ratio, 1.35; 95% CI, 1.09 to 1.68; P = .0065).
High CXCR4 expression in primary
tumor
specimens (n = 35) from AJCC stage IV patients correlated with worse overall median survival (9 months v 23 months; RR, 2.53; 95% CI, 1.19 to 5.40; P = .016).
[MeSH-major]
Colorectal Neoplasms / genetics. Colorectal Neoplasms / pathology. Gene Expression Profiling. Liver Neoplasms / genetics. Liver Neoplasms / secondary.
Neoplasm
Recurrence, Local / genetics. Receptors, CXCR4 / biosynthesis
[MeSH-minor]
Adult. Aged. Aged, 80 and over. Female. Humans. Male. Middle Aged.
Neoplasm
Metastasis / physiopathology. Prognosis. Risk Factors. Signal Transduction. Survival Analysis.
Tumor
Cells, Cultured
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(PMID = 15837989.001).
[ISSN]
0732-183X
[Journal-full-title]
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
[ISO-abbreviation]
J. Clin. Oncol.
[Language]
eng
[Grant]
United States / NCI NIH HHS / CA / R01-CA90848-02
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
[Publication-country]
United States
[Chemical-registry-number]
0 / Receptors, CXCR4
17.
Aneiros-Fernandez J, Caba-Molina M, Arias-Santiago S, Ovalle F, Hernandez-Cortes P, Aneiros-Cachaza J:
Myositis ossificans circumscripta without history of trauma.
J Clin Med Res
; 2010 May 19;2(3):142-4
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Myositis ossificans circumscripta is a form of heterotopic ossification that is
benign
in nature associated to a trauma, but may appear clinically and radiologically as a malignant
neoplasm
.
We discuss some of the difficulties of
diagnosis
and histological evolution of the lesion.
KEYWORDS: Myositis ossificans; Thigh; Differential
diagnosis
; Nontraumatic.
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[Cites]
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[ISSN]
1918-3011
[Journal-full-title]
Journal of clinical medicine research
[ISO-abbreviation]
J Clin Med Res
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Canada
[Other-IDs]
NLM/ PMC3104644
18.
Abdel MP, Papagelopoulos PJ, Morrey ME, Wenger DE, Rose PS, Sim FH:
Surgical management of 121 benign proximal fibula tumors.
Clin Orthop Relat Res
; 2010 Nov;468(11):3056-62
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[Title]
Surgical management of 121
benign
proximal fibula tumors.
Patients with aggressive
benign
tumors in the proximal fibula may require en bloc resection.
QUESTIONS/PURPOSES: We therefore analyzed the incidence of peroneal nerve palsy, knee stability, and local recurrence following surgical treatment
of benign
proximal fibula tumors.
METHODS: We retrospectively reviewed the charts of 120 patients (121 tumors) with histologically confirmed aggressive
benign
tumors of the proximal fibula.
The most common
diagnosis
was osteochondroma (38%) followed by giant cell
tumor
(19%).
[MeSH-minor]
Adolescent. Adult. Child. Child, Preschool. Curettage / adverse effects. Female. Humans.
Joint
Instability / etiology.
Joint
Instability / physiopathology. Knee
Joint
/ physiopathology. Male. Middle Aged.
Neoplasm
Recurrence, Local. Osteotomy / adverse effects. Peroneal Neuropathies / etiology. Range of Motion, Articular. Retrospective Studies. Surgical Wound Dehiscence / etiology. Time Factors. Treatment Outcome. Venous Thrombosis / etiology. Young Adult
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[ISSN]
1528-1132
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2947668
19.
Quaia E, Tona G, Gelain F, Lubin E, Pizzolato R, Boscolo E, Bussoli L:
Integrated fluorine-18 fluorodeoxyglucose (18F-FDG) PET/CT compared to standard contrast-enhanced CT for characterization and staging of pulmonary tumors eligible for surgical resection.
Acta Radiol
; 2008 Nov;49(9):995-1004
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PURPOSE: To compare 18F-FDG PET/CT with standard contrast-enhanced CT for the
diagnosis
and staging of lung neoplasms eligible for surgical resection.
Seventy-three malignant (65 non-small-cell lung carcinomas, one small-cell lung cancer, two carcinoids, and five metastases) and 11
benign
lung tumors (three hamartomas, two sarcoidosis, one amyloidosis, one Wegener granulomatosis, one tuberculosis, and three areas of scarring) were finally diagnosed by histology.
Tumor
staging was based on the revised American
Joint
Committee on Cancer.
[MeSH-major]
Fluorodeoxyglucose F18. Lung Neoplasms /
diagnosis
. Positron-Emission Tomography. Tomography, X-Ray Computed
[MeSH-minor]
Contrast Media. Female. Humans. Image Enhancement. Lung Diseases /
diagnosis
. Male. Middle Aged.
Neoplasm
Staging / methods. Prospective Studies. Sensitivity and Specificity
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(PMID = 18651256.001).
[ISSN]
1600-0455
[Journal-full-title]
Acta radiologica (Stockholm, Sweden : 1987)
[ISO-abbreviation]
Acta Radiol
[Language]
eng
[Publication-type]
Comparative Study; Journal Article
[Publication-country]
Sweden
[Chemical-registry-number]
0 / Contrast Media; 0Z5B2CJX4D / Fluorodeoxyglucose F18
20.
Milot L, Guindi M, Gallinger S, Moulton CA, Brock KK, Dawson LA, Haider MA:
MR imaging correlates of intratumoral tissue types within colorectal liver metastases: a high-spatial-resolution fresh ex vivo radiologic-pathologic correlation study.
Radiology
; 2010 Mar;254(3):747-54
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This SI pattern is unusual for common
benign
liver lesions and may be helpful in the MR imaging
diagnosis
of colorectal liver metastases. (c) RSNA, 2010.
[MeSH-major]
Colorectal Neoplasms / pathology. Liver Neoplasms /
diagnosis
. Liver Neoplasms / secondary. Magnetic Resonance Imaging / methods
[MeSH-minor]
Adult. Aged. Female. Humans. In Vitro Techniques. Linear Models. Male. Middle Aged.
Neoplasm
Staging. Prospective Studies
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(PMID = 20123902.001).
[ISSN]
1527-1315
[Journal-full-title]
Radiology
[ISO-abbreviation]
Radiology
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
21.
He H, Chen G, Zhou L, Liu Y:
A joint detection of CEA and CA-50 levels in saliva and serum of patients with tumors in oral region and salivary gland.
J Cancer Res Clin Oncol
; 2009 Oct;135(10):1315-21
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[Title]
A
joint
detection of CEA and CA-50 levels in saliva and serum of patients with tumors in oral region and salivary gland.
METHODS: The concentrations of salivary CEA and CA-50 were assayed in 80 patients of oral and salivary malignant tumors, 40 patients
of benign
tumors and 80 health controls.
RESULTS: Salivary CEA and CA-50 levels were significantly higher in malignant tumors than in
benign
tumors and in health controls, respectively (P < 0.001).
This may be more useful as prognostic indicators in early
diagnosis
of oral and salivary malignant tumors.
[MeSH-major]
Adenoma / blood. Antigens,
Tumor
-Associated, Carbohydrate / analysis. Carcinoembryonic Antigen / analysis. Mouth Neoplasms / blood. Saliva / chemistry. Salivary Gland Neoplasms / blood
[MeSH-minor]
Adult. Aged. Aged, 80 and over. Case-Control Studies. Enzyme-Linked Immunosorbent Assay. Female. Humans. Immunoradiometric Assay. Male. Middle Aged.
Neoplasm
Staging. Prognosis. Survival Rate. Young Adult
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Proteomics Clin Appl. 2008 Apr;2(4):517-27
[
21136855.001
]
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[
1739620.001
]
[Cites]
Eur J Cancer Prev. 1995 Apr;4(2):129-38
[
7539317.001
]
(PMID = 19322585.001).
[ISSN]
1432-1335
[Journal-full-title]
Journal of cancer research and clinical oncology
[ISO-abbreviation]
J. Cancer Res. Clin. Oncol.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
Germany
[Chemical-registry-number]
0 / Antigens, Tumor-Associated, Carbohydrate; 0 / CA-50 antigen; 0 / Carcinoembryonic Antigen
22.
Gaeta M, Mazziotti S, Minutoli F, Genitori A, Toscano A, Rodolico C, Blandino A:
MR imaging findings of focal myositis: a pseudotumour that may mimic muscle neoplasm.
Skeletal Radiol
; 2009 Jun;38(6):571-8
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[Title]
MR imaging findings of focal myositis: a pseudotumour that may mimic muscle
neoplasm
.
Dynamic enhancement pattern corresponded to the type usually seen in
benign
soft tissue lesions.
CONCLUSION: Focal myositis is an uncommon pseudotumour which should be considered in the differential
diagnosis
of muscular masses and myopathies.
[MeSH-minor]
Adult. Aged.
Diagnosis
, Differential. Female. Humans. Male. Middle Aged. Young Adult
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(PMID = 19255757.001).
[ISSN]
1432-2161
[Journal-full-title]
Skeletal radiology
[ISO-abbreviation]
Skeletal Radiol.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
23.
do Egito Vasconcelos BC, Porto GG, Bessa-Nogueira RV:
Rare benign tumors of the mandibular condyle: report of 2 cases and literature review.
J Oral Maxillofac Surg
; 2007 Sep;65(9):1830-5
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[Title]
Rare
benign
tumors of the mandibular condyle: report of 2 cases and literature review.
[MeSH-minor]
Adult.
Diagnosis
, Differential. Dislocations / etiology. Dislocations / surgery. Facial Asymmetry / etiology. Facial Asymmetry / surgery. Female. Humans.
Neoplasm
Invasiveness. Rare Diseases. Temporomandibular
Joint
Disc / surgery. Temporomandibular
Joint
Disorders / etiology. Temporomandibular
Joint
Disorders / surgery
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(PMID = 17719407.001).
[ISSN]
0278-2391
[Journal-full-title]
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
[ISO-abbreviation]
J. Oral Maxillofac. Surg.
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Review
[Publication-country]
United States
[Number-of-references]
25
24.
Miller IJ, Blank A, Yin SM, McNickle A, Gray R, Gitelis S:
A case of recurrent giant cell tumor of bone with malignant transformation and benign pulmonary metastases.
Diagn Pathol
; 2010;5:62
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[Title]
A case of recurrent giant cell
tumor
of bone with malignant transformation and
benign
pulmonary metastases.
Giant cell
tumor
(GCT) of bone is a locally destructive
tumor
that occurs predominantly in long bones of post-pubertal adolescents and young adults, where it occurs in the epiphysis.
Vascular invasion outside the boundary of the
tumor
can be seen.
Metastasis, with identical morphology to the primary
tumor
, occurs in a few percent of cases, usually to the lung.
[MeSH-major]
Bone Neoplasms / pathology. Cell Transformation, Neoplastic / pathology. Giant Cell
Tumor
of Bone / secondary. Lung Neoplasms / secondary.
Neoplasm
Recurrence, Local. Tibia / pathology
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[ISSN]
1746-1596
[Journal-full-title]
Diagnostic pathology
[ISO-abbreviation]
Diagn Pathol
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
England
[Chemical-registry-number]
0 / Bone Cements
[Other-IDs]
NLM/ PMC2954972
25.
Rubin G, Wolovelsky A, Rinott M, Rozen N:
Osteoid osteoma of the hamate: an unusual cause of ulnar-sided wrist pain.
Orthopedics
; 2010 Jul;33(7):513
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Osteoid osteoma is a
benign
skeletal
neoplasm of
unknown etiology that is composed of osteoid and woven bone.
Its incidence is 11%
of benign
tumors and 3% of all primary bone tumors, with 6% to 13% of all cases occurring in the hand.
Osteoid osteoma of the hamate can produce ulnar-sided wrist pain in the dorsal or volar aspect of the wrist, depending on the location of the
tumor
in the bone.
A
tumor
located in the hook will produce volar pain.
[MeSH-major]
Arthralgia /
diagnosis
. Bone Neoplasms / pathology. Hamate Bone / pathology. Osteoma, Osteoid / pathology. Ulna / pathology
[MeSH-minor]
Humans. Male. Treatment Outcome. Wrist
Joint
/ pathology. Wrist
Joint
/ physiopathology. Wrist
Joint
/ surgery. Young Adult
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[Copyright]
Copyright 2010, SLACK Incorporated.
(PMID = 20608627.001).
[ISSN]
1938-2367
[Journal-full-title]
Orthopedics
[ISO-abbreviation]
Orthopedics
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
26.
Mohler DG, Chiu R, McCall DA, Avedian RS:
Curettage and cryosurgery for low-grade cartilage tumors is associated with low recurrence and high function.
Clin Orthop Relat Res
; 2010 Oct;468(10):2765-73
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Grade 1 chondrosarcomas have little or no metastatic potential and are often difficult to distinguish from painful
benign
enchondromas.
Patients were followed a minimum of 18 months (average, 47.2. months; range, 18-134 months) for evidence of recurrence and for assessment of Musculoskeletal
Tumor
Society (MSTS) functional score.
RESULTS: Two of the 46 patients had recurrences in the original
tumor
site (4.3% recurrence rate), which subsequently were removed by wide excision, and both patients were confirmed to be disease-free 36 and 30 months, respectively, after the second surgery.
[MeSH-minor]
Adolescent. Adult. Aged. Female. Humans. Magnetic Resonance Imaging. Male. Middle Aged.
Neoplasm
Recurrence, Local.
Neoplasm
Staging. Recovery of Function. Retrospective Studies. Time Factors. Treatment Outcome. Young Adult
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[ISSN]
1528-1132
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC3049634
27.
Micheli A, Trapani S, Brizzi I, Campanacci D, Resti M, de Martino M:
Myositis ossificans circumscripta: a paediatric case and review of the literature.
Eur J Pediatr
; 2009 May;168(5):523-9
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At onset, it is difficult to distinguish MOC from a musculoskeletal infection or
neoplasm
, particularly in absence of trauma, and a biopsy is frequently required.
Three months after
diagnosis
, surgical excision was performed.
Our case study confirms the good prognosis of MOC and underlines how this
benign
condition should be considered in children presenting a tender and painful soft-tissue swelling.
[MeSH-major]
Bone and Bones. Musculoskeletal Diseases. Myositis Ossificans /
diagnosis
. Myositis Ossificans / physiopathology
[MeSH-minor]
Anti-Bacterial Agents / therapeutic use. Anti-Inflammatory Agents / therapeutic use. Biopsy. Child.
Diagnosis
, Differential. Humans. Lymphadenitis /
diagnosis
. Magnetic Resonance Imaging. Male. Muscle, Skeletal / metabolism. Muscle, Skeletal / pathology. Necrosis / pathology. Osteoblasts / metabolism. Sarcoma / pathology. Soft Tissue Injuries /
diagnosis
. Soft Tissue Injuries / metabolism. Soft Tissue Injuries / pathology
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[Cites]
Skeletal Radiol. 1992;21(2):87-101
[
1566115.001
]
[Cites]
J Bone Joint Surg Am. 1958 Apr;40-A(2):279-98
[
13539055.001
]
(PMID = 19130083.001).
[ISSN]
1432-1076
[Journal-full-title]
European journal of pediatrics
[ISO-abbreviation]
Eur. J. Pediatr.
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Review
[Publication-country]
Germany
[Chemical-registry-number]
0 / Anti-Bacterial Agents; 0 / Anti-Inflammatory Agents
[Number-of-references]
35
28.
Sailhan F, Chotel F, Parot R, SOFOP:
Chondroblastoma of bone in a pediatric population.
J Bone Joint Surg Am
; 2009 Sep;91(9):2159-68
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BACKGROUND: Chondroblastoma is a rare
benign
bone lesion that occurs in young patients and has a high rate of recurrence.
METHODS: We retrospectively reviewed eighty-seven cases of chondroblastoma in patients with open physes at the time of
diagnosis
and treatment.
[MeSH-major]
Bone Neoplasms / epidemiology. Chondroblastoma / epidemiology. Femur.
Neoplasm
Recurrence, Local / epidemiology. Tibia
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(PMID = 19723993.001).
[ISSN]
1535-1386
[Journal-full-title]
The Journal of bone and joint surgery. American volume
[ISO-abbreviation]
J Bone Joint Surg Am
[Language]
eng
[Publication-type]
Journal Article; Multicenter Study
[Publication-country]
United States
29.
Jones KB, DeYoung BR, Morcuende JA, Buckwalter JA:
Ethanol as a local adjuvant for giant cell tumor of bone.
Iowa Orthop J
; 2006;26:69-76
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[Title]
Ethanol as a local adjuvant for giant cell
tumor
of bone.
Giant cell
tumor
is an aggressive
benign neoplasm
of bone.
No report on its use in a group of patients with giant cell
tumor
is available.
[MeSH-major]
Bone Neoplasms / therapy. Ethanol / therapeutic use. Giant Cell
Tumor
of Bone / therapy
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ETHANOL
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[Cites]
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[ISSN]
1541-5457
[Journal-full-title]
The Iowa orthopaedic journal
[ISO-abbreviation]
Iowa Orthop J
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Chemical-registry-number]
3K9958V90M / Ethanol
[Other-IDs]
NLM/ PMC1888590
30.
Sailon AM, Cappuccino G, Hameed M, Fleegler EJ:
Nodular fasciitis of the hand over the metacarpophalangeal joint: a case report.
Eplasty
; 2008;8:e38
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[Title]
Nodular fasciitis of the hand over the metacarpophalangeal
joint
: a case report.
OBJECTIVE: This study describes a case of nodular fasciitis involving the hand and reviews the
neoplasm
's pertinent clinical, histologic, and pathologic features.
CONCLUSIONS: Nodular fasciitis is a self-limited,
benign
soft tissue
tumor
composed of fibroblasts and myofibroblasts that typically afflicts younger patients and rarely presents in the hand.
Because of its presentation, it can be easily mistaken for a malignant
neoplasm
.
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[Cites]
Orthop Clin North Am. 2006 Jan;37(1):53-63
[
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]
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Histopathology. 2005 Sep;47(3):320-1
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[
7923068.001
]
(PMID = 18725954.001).
[ISSN]
1937-5719
[Journal-full-title]
Eplasty
[ISO-abbreviation]
Eplasty
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2491338
31.
Li JM, Yang ZP, Li ZF, Li X, Carter SR:
Knee reconstruction with preservation of the meniscus in tibial giant cell tumor.
Clin Orthop Relat Res
; 2008 Dec;466(12):3101-7
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[Title]
Knee reconstruction with preservation of the meniscus in tibial giant cell
tumor
.
Giant cell
tumor
of bone sometimes is an aggressive
benign
skeletal
tumor
.
Thus, maintaining
joint
function and achieving adequately wide resection introduces contradictory surgical goals.
We reconstructed 13 knees preserving the meniscus and reconstructing the tibial plateau with an iliac plate autograft after resection of a giant cell
tumor
involving one tibial plateau.
While resecting the
tumor
, the normal anatomic structures of the knee can be preserved or restored in many patients.
[MeSH-major]
Bone Neoplasms / surgery. Giant Cell
Tumor
of Bone / surgery. Orthopedic Procedures / methods. Reconstructive Surgical Procedures / methods
[MeSH-minor]
Adult. Bone Transplantation. Female. Humans. Ilium / transplantation. Male. Menisci, Tibial. Middle Aged.
Neoplasm
Recurrence, Local / epidemiology. Retrospective Studies. Tibia. Transplantation, Autologous. Young Adult
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[Cites]
Clin Orthop Relat Res. 2002 Apr;(397):248-58
[
11953616.001
]
[Cites]
Clin Orthop Relat Res. 2005 Jun;(435):211-8
[
15930941.001
]
[Cites]
J Bone Joint Surg Br. 2004 Mar;86(2):212-6
[
15046435.001
]
[Cites]
J Bone Joint Surg Am. 1970 Jun;52(4):619-64
[
5479455.001
]
[Cites]
J Bone Joint Surg Am. 1975 Mar;57(2):167-73
[
1112843.001
]
[Cites]
J Bone Joint Surg Am. 1982 Jun;64(5):755-61
[
7045129.001
]
[Cites]
Acta Orthop Scand. 1984 Apr;55(2):209-14
[
6369866.001
]
[Cites]
J Bone Joint Surg Am. 1986 Feb;68(2):235-42
[
3511063.001
]
[Cites]
Clin Orthop Relat Res. 1986 Mar;(204):45-58
[
3514036.001
]
[Cites]
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[
3805057.001
]
[Cites]
Clin Orthop Relat Res. 1993 Jan;(286):241-6
[
8425352.001
]
[Cites]
J Bone Joint Surg Am. 1993 Nov;75(11):1648-55
[
8245057.001
]
[Cites]
J Bone Joint Surg Am. 1993 Nov;75(11):1656-62
[
8245058.001
]
[Cites]
Changgeng Yi Xue Za Zhi. 1998 Mar;21(1):37-43
[
9607262.001
]
[Cites]
Clin Orthop Relat Res. 1999 Feb;(359):176-88
[
10078141.001
]
[Cites]
J Bone Joint Surg Am. 1999 Jun;81(6):811-20
[
10391546.001
]
[Cites]
Clin Orthop Relat Res. 2002 Apr;(397):259-70
[
11953617.001
]
(PMID = 18830792.001).
[ISSN]
1528-1132
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2628220
32.
Zhou WQ, Yin HL, Zhang ZY, Yi XM, Ge JP, Zhou SG, Cheng W, Wei W, Ma HQ, Ma HH, Gao JP:
[Expression of VEGF in prostate cancer and its correlation with ET-1].
Zhonghua Nan Ke Xue
; 2008 Nov;14(11):987-92
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OBJECTIVE: To investigate the expressions of VEGF in prostate cancer (PCa) and
benign
prostatic hyperplasia (BPH), their clinical significance and their relationship with that of ET-1.
VEGF and ET-1 may play a
joint
role in its development and progression.
[MeSH-minor]
Aged. Aged, 80 and over. Humans. Male. Middle Aged.
Neoplasm
Metastasis.
Neoplasm
Staging. Prostatic Hyperplasia / metabolism. Prostatic Hyperplasia / pathology
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(PMID = 19102498.001).
[ISSN]
1009-3591
[Journal-full-title]
Zhonghua nan ke xue = National journal of andrology
[ISO-abbreviation]
Zhonghua Nan Ke Xue
[Language]
chi
[Publication-type]
English Abstract; Journal Article
[Publication-country]
China
[Chemical-registry-number]
0 / Endothelin-1; EC 2.7.10.1 / Vascular Endothelial Growth Factor Receptor-1
33.
Batra PS, Luong A, Kanowitz SJ, Sade B, Lee J, Lanza DC, Citardi MJ:
Outcomes of minimally invasive endoscopic resection of anterior skull base neoplasms.
Laryngoscope
; 2010 Jan;120(1):9-16
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Malignant and
benign
tumors were managed in 25 (80.6%) and six (19.4%) cases, respectively.
American
Joint
Committee on Cancer
tumor
staging was T3N0M0 and T4N0M0 in 14 (56%) and 11 (44%) of the malignant cases, respectively.
CONCLUSIONS: This study validated technical feasibility of MIER for diversity
of benign
and malignant ASB histopathology.
[MeSH-minor]
Adolescent. Adult. Aged. Aged, 80 and over. Carcinoma / surgery. Carcinoma, Squamous Cell / surgery. Esthesioneuroblastoma, Olfactory / surgery. Feasibility Studies. Female. Follow-Up Studies. Humans. Male. Melanoma / surgery. Middle Aged.
Neoplasm
Staging. Retrospective Studies. Treatment Outcome
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(PMID = 19877265.001).
[ISSN]
1531-4995
[Journal-full-title]
The Laryngoscope
[ISO-abbreviation]
Laryngoscope
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
34.
Sim IW, Tse LF, Ek ET, Powell GJ, Choong PF:
Salvaging the limb salvage: management of complications following endoprosthetic reconstruction for tumours around the knee.
Eur J Surg Oncol
; 2007 Aug;33(6):796-802
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Tumour types included 38 primary musculoskeletal malignancies, 8 metastatic tumours, 2 bony lymphomas and 2
benign
lesions.
[MeSH-major]
Arthroplasty, Replacement, Knee.
Joint
Diseases / surgery. Knee
Joint
/ surgery. Limb Salvage. Neoplasms / surgery
[MeSH-minor]
Adolescent. Adult. Aged. Amputation. Bone Neoplasms / surgery. Female. Follow-Up Studies. Humans. Intraoperative Complications.
Joint
Prosthesis. Male. Middle Aged. Muscle Neoplasms / surgery.
Neoplasm
Metastasis. Popliteal Artery / injuries. Postoperative Complications. Prosthesis Failure. Reoperation. Retrospective Studies. Surgical Wound Infection / etiology. Survival Rate. Treatment Outcome
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.
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.
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(PMID = 17291709.001).
[ISSN]
0748-7983
[Journal-full-title]
European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
[ISO-abbreviation]
Eur J Surg Oncol
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
35.
Balke M, Streitbuerger A, Budny T, Henrichs M, Gosheger G, Hardes J:
Treatment and outcome of giant cell tumors of the pelvis.
Acta Orthop
; 2009 Oct;80(5):590-6
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METHODS: 20 patients with histologically
benign
GCT of the pelvis were included in this study.
RESULTS: 1 patient with a pubic
tumor
developed a local recurrence 1 year after intralesional resection and additional curettage of the margins.
[MeSH-major]
Bone Neoplasms / surgery. Giant Cell
Tumor
of Bone / surgery. Pelvic Bones
[MeSH-minor]
Adult. Aged. Bone Cements. Bone Transplantation. Curettage. Embolization, Therapeutic / methods. Female. Follow-Up Studies. Humans. Ilium / pathology. Ilium / surgery. Male. Middle Aged.
Neoplasm
Recurrence, Local / prevention & control. Radiotherapy, Adjuvant. Retrospective Studies. Treatment Outcome
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(PMID = 19916695.001).
[ISSN]
1745-3682
[Journal-full-title]
Acta orthopaedica
[ISO-abbreviation]
Acta Orthop
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
[Chemical-registry-number]
0 / Bone Cements
[Other-IDs]
NLM/ PMC2823344
36.
Schwartz AJ, Kabo JM, Eilber FC, Eilber FR, Eckardt JJ:
Cemented distal femoral endoprostheses for musculoskeletal tumor: improved survival of modular versus custom implants.
Clin Orthop Relat Res
; 2010 Aug;468(8):2198-210
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[Title]
Cemented distal femoral endoprostheses for musculoskeletal
tumor
: improved survival of modular versus custom implants.
We excluded two patients with cementless implants, 27 with expandable prostheses, and 39 who had a nontumor
diagnosis
.
The
tumor
was classified as Stage IIA/IIB in 122 patients, Stage IA/IB or
benign
in 43, and Stage III or metastatic in 21.
[MeSH-major]
Bone Neoplasms / surgery. Femur / surgery.
Joint
Prosthesis. Prosthesis Failure. Reconstructive Surgical Procedures / instrumentation
[MeSH-minor]
Adolescent. Adult. Aged. Cementation. Child. Female. Humans. Male. Middle Aged.
Neoplasm
Staging. Prosthesis Design. Reoperation. Retrospective Studies. Young Adult
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[Cites]
Adolesc Med. 1999 Oct;10(3):451-8, xii
[
10611942.001
]
[Cites]
Clin Orthop Relat Res. 2005 Sep;438:51-9
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]
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]
[Cites]
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(PMID = 20033359.001).
[ISSN]
1528-1132
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2895832
37.
Al Yami A, Griffin AM, Ferguson PC, Catton CN, Chung PW, Bell RS, Wunder JS, O'Sullivan B:
Positive surgical margins in soft tissue sarcoma treated with preoperative radiation: is a postoperative boost necessary?
Int J Radiat Oncol Biol Phys
; 2010 Jul 15;77(4):1191-7
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There was no difference in baseline
tumor
characteristics between the two groups.
Given that higher radiation doses placed patients at greater risk for late complications such as fracture, fibrosis, edema, and
joint
stiffness, judicious avoidance of the postoperative boost while maintaining an equivalent rate of local control can reduce the risk of these difficult-to-treat morbidities.
[MeSH-minor]
Adult. Aged. Aged, 80 and over. Amputation. Female. Histiocytoma,
Benign
Fibrous / pathology. Histiocytoma,
Benign
Fibrous / prevention & control. Histiocytoma,
Benign
Fibrous / radiotherapy. Histiocytoma,
Benign
Fibrous / surgery. Humans. Leiomyosarcoma / pathology. Leiomyosarcoma / prevention & control. Leiomyosarcoma / radiotherapy. Leiomyosarcoma / surgery. Limb Salvage. Liposarcoma / pathology. Liposarcoma / prevention & control. Liposarcoma / radiotherapy. Liposarcoma / surgery. Male. Middle Aged.
Neoplasm
Recurrence, Local / prevention & control.
Neoplasm
, Residual. Postoperative Care. Radiotherapy Dosage. Retreatment. Young Adult
Genetic Alliance.
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[Copyright]
Copyright 2010 Elsevier Inc. All rights reserved.
[CommentIn]
Int J Radiat Oncol Biol Phys. 2011 Jul 1;80(3):959; author reply 959-60
[
21621120.001
]
(PMID = 20056340.001).
[ISSN]
1879-355X
[Journal-full-title]
International journal of radiation oncology, biology, physics
[ISO-abbreviation]
Int. J. Radiat. Oncol. Biol. Phys.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
38.
Puhaindran ME, Healey JH, Athanasian EA:
Single ray amputation for tumors of the hand.
Clin Orthop Relat Res
; 2010 May;468(5):1390-5
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The role of this procedure in the management of aggressive
benign
or malignant hand tumors has been described only in case reports and small case series.
The other was treated with radiotherapy alone, as local
tumor
control would have required a hand amputation.
Functional assessment based on the Musculoskeletal
Tumor
Society staging system showed an average of 27.5 (range, 21-30).
[MeSH-minor]
Adolescent. Adult. Aged. Aged, 80 and over. Child. Female. Follow-Up Studies. Humans. Male. Middle Aged.
Neoplasm
Recurrence, Local. Retrospective Studies. Time Factors. Treatment Outcome. Young Adult
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[
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[ISSN]
1528-1132
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Comparative Study; Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2853661
39.
Jeys LM, Suneja R, Chami G, Grimer RJ, Carter SR, Tillman RM:
Impending fractures in giant cell tumours of the distal femur: incidence and outcome.
Int Orthop
; 2006 Apr;30(2):135-8
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Giant cell tumours are rare bone tumours that are characteristically
benign
but locally aggressive, most frequently occurring in the distal femur with pathological fractures being common.
[MeSH-major]
Femoral Fractures / epidemiology. Femoral Fractures / physiopathology. Femoral Neoplasms / physiopathology. Giant Cell
Tumor
of Bone / physiopathology
[MeSH-minor]
Adolescent. Adult. Aged. Analysis of Variance. Female. Humans. Incidence. Male. Middle Aged.
Neoplasm
Recurrence, Local. Prospective Studies. Risk Factors
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[ISSN]
0341-2695
[Journal-full-title]
International orthopaedics
[ISO-abbreviation]
Int Orthop
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
[Other-IDs]
NLM/ PMC2532068
40.
Yanagawa T, Watanabe H, Shinozaki T, Takagishi K:
Curettage of benign bone tumors without grafts gives sufficient bone strength.
Acta Orthop
; 2009 Feb;80(1):9-13
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[Title]
Curettage
of benign
bone tumors without grafts gives sufficient bone strength.
BACKGROUND AND PURPOSE: The defect that results after curettage of a bone
tumor
is usually filled in the same way.
We report the outcome in patients with
benign
bone tumors that were treated with curettage but no filling.
PATIENTS AND METHODS: We retrospectively studied 78 patients (mean age at the time of operation was 27 (6-73) years, 44 men) who had had a
benign
bone
tumor
curetted with no filling of the defect.
The commonest
tumor
types were giant cell
tumor
of bone (27), fibrous dysplasia (13), enchondroma (9), and simple bone cyst (7).
Local recurrence occurred in 9 patients; 7 of them had a giant cell
tumor
.
[MeSH-minor]
Adolescent. Adult. Aged. Bone Cysts / surgery. Bone Remodeling / physiology. Follow-Up Studies. Giant Cell
Tumor
of Bone / surgery. Humans. Middle Aged.
Neoplasm
Recurrence, Local / surgery. Retrospective Studies. Treatment Outcome. Young Adult
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[CommentIn]
Acta Orthop. 2009 Feb;80(1):2-3
[
19297784.001
]
(PMID = 19234882.001).
[ISSN]
1745-3682
[Journal-full-title]
Acta orthopaedica
[ISO-abbreviation]
Acta Orthop
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Sweden
[Other-IDs]
NLM/ PMC2823236
41.
Lehnhardt M, Daigeler A, Homann HH, Hauser J, Langer S, SteinstrƤsser L, Soimaru C, Puls A, Steinau HU:
[Importance of specialized centers in diagnosis and treatment of extremity-soft tissue sarcomas. Review of 603 cases].
Chirurg
; 2009 Apr;80(4):341-7
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[Title]
[Importance of specialized centers in
diagnosis
and treatment of extremity-soft tissue sarcomas. Review of 603 cases].
Correct histopathologic
diagnosis
is essential for adequate treatment of soft tissue sarcomas.
Due to the disorder's rarity, multitude of subgroups, sometimes varying histopathologic appearance, and occasionally inadequate biopsy specimens,
diagnosis
and grading are challenging.
The records of 603 patients with soft tissue tumors of the extremities were reviewed concerning mismatches in primary and definite diagnoses relating to entity, evaluation of primary or recurrent
tumor
specimens, and the diagnosing pathology institution.
In the eight most frequent sarcoma types, malignant peripheral nerve sheath tumors and leiomyosarcoma had the highest rates of false primary
diagnosis
, 78.4% and 74.2% of cases, respectively.
[MeSH-major]
Cancer Care Facilities. Extremities / surgery. Hospitals, Special. Hospitals, University. Sarcoma /
diagnosis
. Sarcoma / surgery. Soft Tissue Neoplasms /
diagnosis
. Soft Tissue Neoplasms / surgery
[MeSH-minor]
Adolescent. Adult. Aged. Aged, 80 and over. Chemotherapy, Adjuvant. Child. Combined Modality Therapy. Diagnostic Errors. Female. Germany. Histiocytoma,
Benign
Fibrous /
diagnosis
. Histiocytoma,
Benign
Fibrous / pathology. Histiocytoma,
Benign
Fibrous / surgery. Humans. Leiomyosarcoma /
diagnosis
. Leiomyosarcoma / pathology. Leiomyosarcoma / surgery. Liposarcoma /
diagnosis
. Liposarcoma / pathology. Liposarcoma / surgery. Male. Middle Aged.
Neoplasm
Staging. Nerve Sheath Neoplasms /
diagnosis
. Nerve Sheath Neoplasms / pathology. Nerve Sheath Neoplasms / surgery. Radiotherapy, Adjuvant. Referral and Consultation. Retrospective Studies. Young Adult
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42.
Jawad MU, Scully SP:
In brief: classifications in brief: enneking classification: benign and malignant tumors of the musculoskeletal system.
Clin Orthop Relat Res
; 2010 Jul;468(7):2000-2
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[Title]
In brief: classifications in brief: enneking classification:
benign
and malignant tumors of the musculoskeletal system.
[MeSH-minor]
Humans.
Neoplasm
Metastasis.
Neoplasm
Staging
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[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
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Journal Article
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United States
[Other-IDs]
NLM/ PMC2882012
43.
Skubitz KM, Manivel JC:
Giant cell tumor of the uterus: case report and response to chemotherapy.
BMC Cancer
; 2007;7:46
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[Title]
Giant cell
tumor
of the uterus: case report and response to chemotherapy.
BACKGROUND: Giant cell
tumor
(GCT) is usually a
benign
but locally aggressive primary bone
neoplasm
in which monocytic macrophage/osteoclast precursor cells and multinucleated osteoclast-like giant cells infiltrate the
tumor
.
The etiology of GCT is unknown, however the
tumor
cells of GCT have been reported to produce chemoattractants that can attract osteoclasts and osteoclast precursors.
[MeSH-minor]
Angiogenesis Inhibitors / administration & dosage. Antibiotics, Antineoplastic / administration & dosage. Antibodies, Monoclonal / administration & dosage. Antibodies, Monoclonal, Humanized. Antineoplastic Agents, Alkylating / administration & dosage. Bevacizumab. Combined Modality Therapy. Doxorubicin / administration & dosage. Female. Humans. Hysterectomy. Ifosfamide / administration & dosage. Lung Neoplasms /
diagnosis
. Lung Neoplasms / drug therapy. Lung Neoplasms / secondary. Middle Aged. Treatment Outcome
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DOXORUBICIN
.
Hazardous Substances Data Bank.
IFOSFAMIDE
.
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[ISSN]
1471-2407
[Journal-full-title]
BMC cancer
[ISO-abbreviation]
BMC Cancer
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Review
[Publication-country]
England
[Chemical-registry-number]
0 / Angiogenesis Inhibitors; 0 / Antibiotics, Antineoplastic; 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Humanized; 0 / Antineoplastic Agents, Alkylating; 2S9ZZM9Q9V / Bevacizumab; 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
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57
[Other-IDs]
NLM/ PMC1832205
44.
Brisse H, Orbach D, Klijanienko J, FrƩneaux P, Neuenschwander S:
Imaging and diagnostic strategy of soft tissue tumors in children.
Eur Radiol
; 2006 May;16(5):1147-64
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The
diagnosis
of a soft tissue mass in children is a common clinical situation.
Most of the lesions are
benign
and can be treated conservatively or by non-mutilating surgery.
Nevertheless, the possibility of a malignant soft tissue
tumor
must be systematically considered.
The most frequent
benign
soft tissue lesions in children are vascular lesions, fibrous and fibrohistiocytic tumors and pseudotumors, whereas rhabdomyosarcomas account for 50% of all soft tissue sarcomas.
A child presenting an atypical soft tissue mass should be managed by a multidisciplinary centre, and primary resection must be proscribed until a definite
diagnosis
has been established.
The role of imaging is essential either to confirm the
benign
nature of the mass or to give arguments to perform a diagnostic biopsy.
Clinical examination, conventional radiography and ultrasound with Doppler represent the first-line examinations and are sometimes sufficient to assess a
diagnosis
.
[MeSH-major]
Diagnostic Imaging. Soft Tissue Neoplasms /
diagnosis
[MeSH-minor]
Adolescent. Age Factors. Child. Child, Preschool. Decision Trees. Humans. Infant. Infant, Newborn.
Neoplasm
Staging
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11594280.001
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15459325.001
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[
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Plast Reconstr Surg. 2001 Jun;107(7):1647-54
[
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]
(PMID = 16411083.001).
[ISSN]
0938-7994
[Journal-full-title]
European radiology
[ISO-abbreviation]
Eur Radiol
[Language]
eng
[Publication-type]
Journal Article; Review
[Publication-country]
Germany
[Number-of-references]
108
45.
Bakotic B, Ackerman AB:
Staging of melanoma: a critique in historical perspective: part I.
Am J Dermatopathol
; 2005 Apr;27(2):160-4
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That the method employed for achieving that desideratum, which had as its animating force a longing to determine prognosis for an individual patient with that malignant
neoplasm
, failed miserably can be inferred from the fact that successive efforts every few years by teams of supposed authorities, such as those of the American
Joint
Committee on Cancer (AJCC), resulted in a new system for staging that bore little resemblance to the one immediately before it or the one that was to come after it.
The job of a pathologist is to render an accurate
diagnosis
(which, in itself, has implications prognostic for a patient, eg, "
benign
" or "malignant"), not to speculate about prognosis.
[MeSH-major]
Melanoma / history. Melanoma / pathology.
Neoplasm
Staging / history. Skin Neoplasms / history. Skin Neoplasms / pathology
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(PMID = 15798444.001).
[ISSN]
0193-1091
[Journal-full-title]
The American Journal of dermatopathology
[ISO-abbreviation]
Am J Dermatopathol
[Language]
eng
[Publication-type]
Historical Article; Journal Article
[Publication-country]
United States
46.
Song JW, DU LL, Zhao XW, Jing JX, Han CZ, Cui Y, Liu JW, Hao HL, Wang ZG, Mi ZG:
[Expression and clinical significance of nuclear matrix protein 22 and cytokeratin 18 in transitional cell carcinoma of the bladder].
Zhonghua Zhong Liu Za Zhi
; 2009 Apr;31(4):274-7
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METHODS: Urinary NMP22 and CK18 levels of 293 patients with transitional cell carcinoma of the bladder, 400 patients with non-transitional cell carcinoma of the bladder, and 105 bladder
benign
disease were analysed by enzyme-linked-immunosorbent assay (ELISA).
RESULTS: The levels of urinary NMP22 and CK18 in the patients with transitional cell carcinoma of the bladder (M = 17.3 U/ml, M(CK18) = 484.2 U/L) were significantly higher than those in the non-transitional cell carcinoma of the bladder (M = 6.8 U/ml, M(CK18) = 156.0 U/L) and the
benign
disease group (M(NMP22) = 2.3 U/ml, M(CK18) = 66.6 U/L) (P < 0.001).
The
joint
sensitivity of the two markers was 91.7%.
CONCLUSION: NMP22 and CK18 are useful
tumor
marker for
diagnosis
of transitional cell carcinoma of the bladder and for monitoring the state of illness.
The
joint
use of the two markers can improve the sensitivity of cancer detection.
NMP22 and CK18 may become a new class of
tumor
markers, and to be the basis for development of a new assay with an increased efficacy for the detection and treatment of bladder cancer.
[MeSH-minor]
Adolescent. Adult. Aged. Aged, 80 and over. Biomarkers,
Tumor
/ urine. Carcinoma, Renal Cell / urine. Child. Female. Follow-Up Studies. Humans. Male. Middle Aged.
Neoplasm
Metastasis.
Neoplasm
Recurrence, Local / urine.
Neoplasm
Staging. Prognosis. Sensitivity and Specificity. Young Adult
Genetic Alliance.
consumer health - Transitional cell carcinoma
.
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consumer health - Bladder Cancer
.
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(PMID = 19615282.001).
[ISSN]
0253-3766
[Journal-full-title]
Zhonghua zhong liu za zhi [Chinese journal of oncology]
[ISO-abbreviation]
Zhonghua Zhong Liu Za Zhi
[Language]
chi
[Publication-type]
English Abstract; Journal Article
[Publication-country]
China
[Chemical-registry-number]
0 / Biomarkers, Tumor; 0 / Keratin-18; 0 / Nuclear Proteins; 0 / nuclear matrix protein 22
47.
Gelabert-GonzĆ”lez M, GarcĆa-Allut A:
Spinal extradural angiolipoma: report of two cases and review of the literature.
Eur Spine J
; 2009 Mar;18(3):324-35
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Spinal angiolipomas are
benign
uncommon
neoplasm
composed of mature lipocytes admixed with abnormal blood vessels.
Prior to
diagnosis
40.6% of the patients had weakness of the lower limbs.
The interval between the initial symptoms and
tumor diagnosis
ranged from 1 day to 17 years (mean 20.2 months).
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[ISSN]
1432-0932
[Journal-full-title]
European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
[ISO-abbreviation]
Eur Spine J
[Language]
eng
[Publication-type]
Case Reports; Journal Article; Review
[Publication-country]
Germany
[Number-of-references]
99
[Other-IDs]
NLM/ PMC2899409
48.
Sanatkumar S, Rajagopalan N, Mallikarjunaswamy B, Srinivasalu S, Sudhir NP, Usha K:
Benign fibrous histiocytoma of the distal radius with congenital dislocation of the radial head: a case report.
J Orthop Surg (Hong Kong)
; 2005 Apr;13(1):83-7
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[Title]
Benign
fibrous histiocytoma of the distal radius with congenital dislocation of the radial head: a case report.
Benign
fibrous histiocytoma is such a rare tumour that only a few cases have been reported in the literature.
A patient with an apparently
benign
lesion of the distal radius, along with congenital dislocation of the radial head, was presented at St. John's Medical College Hospital in Bangalore, India.
[MeSH-major]
Amputation. Bone Neoplasms / surgery. Histiocytoma,
Benign
Fibrous / surgery.
Neoplasm
Recurrence, Local / surgery. Orthopedic Procedures / adverse effects
[MeSH-minor]
Adolescent. Fibula / transplantation. Humans.
Joint
Dislocations. Male. Radius. Reoperation. Upper Extremity
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(PMID = 15872408.001).
[ISSN]
1022-5536
[Journal-full-title]
Journal of orthopaedic surgery (Hong Kong)
[ISO-abbreviation]
J Orthop Surg (Hong Kong)
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
England
49.
McGough RL, Rutledge J, Lewis VO, Lin PP, Yasko AW:
Impact severity of local recurrence in giant cell tumor of bone.
Clin Orthop Relat Res
; 2005 Sep;438:116-22
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[Title]
Impact severity of local recurrence in giant cell
tumor
of bone.
We retrospectively reviewed 183 consecutive patients diagnosed with giant cell
tumor
at the three most common sites (distal femur, proximal tibia, and distal radius) to determine the pattern of local
tumor
recurrence and the impact severity of the recurrence on adjacent
joint
function.
The primary
tumor
was treated in all patients with intralesional excision of
tumor
by curettage.
Incomplete initial surgery, a delay in
diagnosis
of the recurrence of greater than 6 months, and subchondral recurrence of
tumor
were contributing factors in the failure to salvage the
joint
.
Despite its
benign
histology, giant cell
tumor
of bone is an aggressive
tumor
that demands meticulous attention to surgical detail and close postoperative surveillance for successful local
tumor
control and durable,
joint
-preserving function.
[MeSH-major]
Bone Neoplasms / pathology. Giant Cell
Tumor
of Bone / pathology.
Neoplasm
Recurrence, Local
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.
COS Scholar Universe.
author profiles
.
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(PMID = 16131879.001).
[ISSN]
0009-921X
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
50.
Hauptmann K, Melcher I, Schaser KD:
[Differential diagnosis of intramedullary osteosarcomas].
Pathologe
; 2008 Nov;29 Suppl 2:240-4
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[Title]
[Differential
diagnosis
of intramedullary osteosarcomas].
The many subtypes and variants of these tumors often make the differential
diagnosis
difficult.
Low-grade central osteosarcomas are a completely different
tumor
group.
Due to their strong similarity to
benign
bone tumors they are frequently misdiagnosed as such.
The correct
diagnosis
followed by radical surgery, however, is essential to reduce the high risk of local recurrences, typically seen for of these lesions.
[MeSH-minor]
Biopsy. Bone and Bones / diagnostic imaging. Bone and Bones / pathology.
Diagnosis
, Differential. Humans.
Neoplasm
Recurrence, Local / diagnostic imaging.
Neoplasm
Recurrence, Local / pathology. Prognosis. Radiography
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[ISSN]
1432-1963
[Journal-full-title]
Der Pathologe
[ISO-abbreviation]
Pathologe
[Language]
ger
[Publication-type]
Journal Article; Review
[Publication-country]
Germany
[Number-of-references]
16
51.
Naka N, Joyama S, Tsukamoto Y, Yoshioka K, Hashimoto N, Ujiiye T, Hayashi T, Kawase M, Mano M, Ishiguro S, Myoui A, Ueda T, Yoshikawa H, Araki N, Itoh K:
Quantification of SSX mRNA expression in human bone and soft tissue tumors using nucleic acid sequence-based amplification.
J Mol Diagn
; 2005 May;7(2):187-97
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The copy numbers of SSX mRNA per mug of total RNA in
tumor
tissues were widely distributed, ranging logarithmically from 0.6 to 6.6.
We found that malignant tumors showed significantly higher expression of SSX mRNA than
benign
tumors (P < 0.0001).
[MeSH-major]
Bone Neoplasms / genetics.
Neoplasm
Proteins / genetics. RNA, Messenger / analysis. Repressor Proteins / genetics. Self-Sustained Sequence Replication. Soft Tissue Neoplasms / genetics
[MeSH-minor]
Adolescent. Adult. Aged. Animals. COS Cells. Child. Female. Gene Expression. Humans. Male. Middle Aged. RNA,
Neoplasm
/ analysis. RNA,
Neoplasm
/ metabolism
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(PMID = 15858142.001).
[ISSN]
1525-1578
[Journal-full-title]
The Journal of molecular diagnostics : JMD
[ISO-abbreviation]
J Mol Diagn
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
[Chemical-registry-number]
0 / Neoplasm Proteins; 0 / RNA, Messenger; 0 / RNA, Neoplasm; 0 / Repressor Proteins; 164289-47-8 / synovial sarcoma X breakpoint proteins
[Other-IDs]
NLM/ PMC1867521
52.
de Prado Prieto L, GarcĆa Olmos L, RodrĆguez SalvanĆ©s F, Otero Puime A:
[Evaluation of referrals in primary care].
Aten Primaria
; 2005 Feb 28;35(3):146-51
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The most common conditions referred, 25.6% of all referrals, are gynecologist check, blindness, other illnesses of subcutaneous cellular tissue, arthrosis,
joint
pain, diabetes,
benign neoplasm
of skin, depression and hypoacusis.
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(PMID = 15737271.001).
[ISSN]
0212-6567
[Journal-full-title]
Atencion primaria
[ISO-abbreviation]
Aten Primaria
[Language]
SPA
[Publication-type]
English Abstract; Journal Article; Multicenter Study
[Publication-country]
Spain
53.
Weber K, Damron TA, Frassica FJ, Sim FH:
Malignant bone tumors.
Instr Course Lect
; 2008;57:673-88
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The primary symptom of a patient with a malignant bone
tumor
is pain, which often occurs at rest or at night.
There are also characteristic findings on physical examination such as swelling or decreased
joint
range of motion.
Patients with a likely malignancy require thorough staging to determine the extent of disease and a well-planned biopsy for accurate
diagnosis
.
Knowledge of specific
tumor
characteristics and treatment options for osteosarcoma, Ewing's sarcoma, chondrosarcoma, malignant fibrous histiocytoma, chordoma, and adamantinoma is important.
Secondary sarcomas can occur in previously
benign
bone lesions and require aggressive treatment.
[MeSH-minor]
Global Health. Humans. Morbidity.
Neoplasm
Staging / methods. Prognosis
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(PMID = 18399615.001).
[ISSN]
0065-6895
[Journal-full-title]
Instructional course lectures
[ISO-abbreviation]
Instr Course Lect
[Language]
eng
[Publication-type]
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
[Publication-country]
United States
[Number-of-references]
42
54.
Mitra R:
Osteitis Condensans Ilii.
Rheumatol Int
; 2010 Jan;30(3):293-6
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Osteitis Condensans Ilii (OCI) is a
benign
cause of axial low back pain.
The location of the sclerosis has been traditionally confined to the ilium and may give the false impression of sacro-iliac
joint
involvement.
[MeSH-major]
Ilium / pathology. Ilium / physiopathology. Low Back Pain / etiology. Low Back Pain / physiopathology. Osteitis /
diagnosis
. Osteitis / physiopathology
[MeSH-minor]
Anti-Inflammatory Agents, Non-Steroidal / therapeutic use.
Diagnosis
, Differential. Humans.
Neoplasm
Metastasis /
diagnosis
. Radiography. Radiology. Sacroiliac
Joint
/ diagnostic imaging. Sacroiliac
Joint
/ pathology. Sacroiliac
Joint
/ physiopathology. Spondylitis, Ankylosing /
diagnosis
. Steroids / therapeutic use
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Semin Musculoskelet Radiol. 2008 Mar;12(1):72-82
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[ISSN]
1437-160X
[Journal-full-title]
Rheumatology international
[ISO-abbreviation]
Rheumatol. Int.
[Language]
eng
[Publication-type]
Journal Article; Review
[Publication-country]
Germany
[Chemical-registry-number]
0 / Anti-Inflammatory Agents, Non-Steroidal; 0 / Steroids
[Number-of-references]
24
55.
Orhan Z, Oktas B, Yildirim U:
An unusual presentation of peroneal neuropathy secondary to pigmented villonodular synovitis: a case report.
Knee Surg Sports Traumatol Arthrosc
; 2009 May;17(5):518-20
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Pigmented villonodular synovitis (PVS) is a
benign
proliferative disorder of unknown origin that affects synovial joints, most commonly the knee.
The
joint
knee can be affected by localized or diffuse form.
Although this disease is categorized as an inflammatory process rather than a
neoplasm
, it may be locally destructive and involve muscles, tendons, bone and skin.
[MeSH-major]
Peroneal Neuropathies /
diagnosis
. Peroneal Neuropathies / etiology. Synovitis, Pigmented Villonodular / complications. Synovitis, Pigmented Villonodular /
diagnosis
[MeSH-minor]
Humans. Knee
Joint
/ pathology. Knee
Joint
/ surgery. Magnetic Resonance Imaging. Male. Middle Aged. Orthopedic Procedures / methods. Peroneal Nerve / pathology. Peroneal Nerve / surgery
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[Cites]
Knee. 2007 Oct;14 (5):390-4
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Clin Orthop Relat Res. 1996 Apr;(325):174-80
[
8998871.001
]
(PMID = 19205665.001).
[ISSN]
1433-7347
[Journal-full-title]
Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA
[ISO-abbreviation]
Knee Surg Sports Traumatol Arthrosc
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
Germany
56.
Zustin J, Akpalo H, Gambarotti M, Priemel M, Rueger JM, Luebke AM, Reske D, Lange C, Pueschel K, Lohmann C, Rüther W, Amling M, Alberghini M:
Phenotypic diversity in chondromyxoid fibroma reveals differentiation pattern of tumor mimicking fetal cartilage canals development: an immunohistochemical study.
Am J Pathol
; 2010 Sep;177(3):1072-8
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[Title]
Phenotypic diversity in chondromyxoid fibroma reveals differentiation pattern of
tumor
mimicking fetal cartilage canals development: an immunohistochemical study.
Chondromyxoid fibroma represents a rare
benign
cartilaginous
tumor
of young patients occurring in a subcortical metaphyseal location.
Based on the observed substantial morphological similarity between the cartilage canals and chondromyxoid fibroma, we suggest that the chondromyxoid fibroma represents a
neoplasm
originating from or mimicking the fetal cartilage canals within the immature cartilage.
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Am J Clin Pathol. 2001 Aug;116(2):271-7
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[ISSN]
1525-2191
[Journal-full-title]
The American journal of pathology
[ISO-abbreviation]
Am. J. Pathol.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2928941
57.
Arroud M, Afifi MA, Chbani L, Riffi AA, Bouabdallah Y:
Giant-cell tumor of the fourth metacarpal bone in children: case report.
J Pediatr Orthop B
; 2010 Jan;19(1):86-9
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[Title]
Giant-cell
tumor
of the fourth metacarpal bone in children: case report.
Giant-cell
tumor
is a rare
benign
tumor
that generally arises in long bones of the lower extremity in adults.
We highlight the rarity of this
neoplasm
in childhood and discuss epidemiological, clinical, radiological, and therapeutical characteristics of this pathology.
[MeSH-major]
Bone Neoplasms / pathology. Giant Cell
Tumor
of Bone / pathology. Metacarpal Bones / pathology
[MeSH-minor]
Child. Humans. Male. Metacarpophalangeal
Joint
/ physiopathology. Metacarpophalangeal
Joint
/ surgery. Range of Motion, Articular / physiology. Reconstructive Surgical Procedures. Treatment Outcome
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[CommentIn]
J Pediatr Orthop B. 2010 May;19(3):285-6
[
20375665.001
]
(PMID = 19898253.001).
[ISSN]
1473-5865
[Journal-full-title]
Journal of pediatric orthopedics. Part B
[ISO-abbreviation]
J Pediatr Orthop B
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
58.
Meller I, Weinbroum A, Bickels J, Dadia S, Nirkin A, Merimsky O, Issakov J, Flusser G, Marouani N, Cohen N, Kollender Y:
Fifteen years of bone tumor cryosurgery: a single-center experience of 440 procedures and long-term follow-up.
Eur J Surg Oncol
; 2008 Aug;34(8):921-7
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[Title]
Fifteen years of bone
tumor
cryosurgery: a single-center experience of 440 procedures and long-term follow-up.
BACKGROUND: This summary of a single center's extensive cumulative experience in bone
tumor
cryosurgery assesses the long-term outcome of bone conservation surgery in which adjuvant cryosurgery plays a pivotal role.
Two-thirds of the series comprised a variety of primary
benign
-aggressive and low-grade malignant lesions, and one-third were primary high-grade and metastatic bone tumors.
There were three cases of transient nerve palsies in areas other than the sacrum, and four cases of late osteoarthritis of an adjacent
joint
.
The functional outcome for the 372 patients with no evidence of disease was almost 100% "good" and "excellent" (American Musculo-skeletal
Tumor
Society System).
CONCLUSIONS: Bone cryosurgery is a safe and effective limb-,
joint
- and even epiphysis-sparing surgical technique in suitable types of bone tumors, temporarily or permanently obviating the need for resection surgery.
[MeSH-major]
Bone Neoplasms / surgery. Cryosurgery.
Neoplasm
Recurrence, Local
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(PMID = 18158228.001).
[ISSN]
1532-2157
[Journal-full-title]
European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
[ISO-abbreviation]
Eur J Surg Oncol
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
England
59.
Wang Z, Guo Z, Li J, Li XD, Sang HX:
Functional outcomes and complications of reconstruction of the proximal humerus after intra-articular tumor resection.
Orthop Surg
; 2010 Feb;2(1):19-26
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[Title]
Functional outcomes and complications of reconstruction of the proximal humerus after intra-articular
tumor
resection.
OBJECTIVE: To evaluate functional outcomes and complications of reconstruction of the proximal humerus after intra-articular
tumor
resection.
METHODS: Twenty-five patients who underwent Malawer I type resection and reconstruction of the proximal humerus for treatment of malignant or invasive
benign
tumors from August 1999 to August 2005 were evaluated.
A variety of reconstructive procedures, including modular
tumor
prosthesis, osteoarticular allograft, and allograft-prosthetic composite (APC), were performed after resection of
tumor
.
The modified Musculoskeletal
Tumor
Society (MSTS) evaluation system was used to assess limb functional outcome.
RESULTS: The study group consisted of 10 male and 15 female patients, among which there were 20 malignant and 5
benign
tumors.
Joint
instability and subluxation were serious complications affecting shoulder function in 10 patients.
[MeSH-major]
Arthroplasty, Replacement / methods. Bone Neoplasms / surgery. Humerus / surgery. Neoplasms, Connective Tissue / surgery. Shoulder
Joint
/ surgery
[MeSH-minor]
Adolescent. Adult. Child. Female. Humans. Lymphoma / mortality. Lymphoma / pathology. Lymphoma / surgery. Male. Middle Aged.
Neoplasm
Metastasis.
Neoplasm
Recurrence, Local. Postoperative Complications / epidemiology. Recovery of Function. Retrospective Studies. Treatment Outcome. Young Adult
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[Copyright]
Ā© 2010 Tianjin Hospital and Blackwell Publishing Asia Pty Ltd.
(PMID = 22009903.001).
[ISSN]
1757-7861
[Journal-full-title]
Orthopaedic surgery
[ISO-abbreviation]
Orthop Surg
[Language]
eng
[Publication-type]
Evaluation Studies; Journal Article
[Publication-country]
Australia
60.
Oliveira RC, Marques KD, MendonƧa AR, MendonƧa EF, Silva MR, Batista AC, Ribeiro-Rotta RF:
Chondrosarcoma of the temporomandibular joint: a case report in a child.
J Orofac Pain
; 2009;23(3):275-81
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[Title]
Chondrosarcoma of the temporomandibular
joint
: a case report in a child.
This article reports a rare case of a temporomandibular
joint
(TMJ) chondrosarcoma in a child.
Chondrosarcoma is a malignant cartilaginous
neoplasm
that resembles synovial chondromatosis.
Microscopic findings showed a
tumor
exhibiting cartilaginous tissue proliferation with cellular pleomorphism, nuclear hyperchromasia, and mixoid changes in the matrix.
It is concluded that cartilaginous lesions in the jaws must be regarded with suspicion, since
benign
and malignant lesions may show similar clinical features.
[MeSH-major]
Chondrosarcoma / pathology. Temporomandibular
Joint
Disorders / pathology
[MeSH-minor]
Child. Cyclin B / analysis. Cyclin B1.
Diagnosis
, Differential. Female. Humans. Immunohistochemistry. Ki-67 Antigen / analysis. Mandibular Condyle / pathology. Temporomandibular
Joint
/ pathology
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(PMID = 19639107.001).
[ISSN]
1064-6655
[Journal-full-title]
Journal of orofacial pain
[ISO-abbreviation]
J Orofac Pain
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
[Chemical-registry-number]
0 / CCNB1 protein, human; 0 / Cyclin B; 0 / Cyclin B1; 0 / Ki-67 Antigen
61.
Donthineni R, Boriani L, Ofluoglu O, Bandiera S:
Metastatic behaviour of giant cell tumour of the spine.
Int Orthop
; 2009 Apr;33(2):497-501
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When there is a recurrence of GCT, with or without metastases, the local and possibly the metastases should be biopsied to confirm the original
diagnosis
.
Progression
of benign
GCT into an aggressive sarcoma has been documented, and the method of management should be altered.
[MeSH-major]
Bone Neoplasms / pathology. Giant Cell
Tumor
of Bone / secondary. Lung Neoplasms / secondary.
Neoplasm
Recurrence, Local / pathology
[MeSH-minor]
Adolescent. Adult. Biopsy, Needle. Combined Modality Therapy. Disease-Free Survival. Female. Humans. Immunohistochemistry. Magnetic Resonance Imaging. Male. Middle Aged.
Neoplasm
Invasiveness / pathology.
Neoplasm
Staging. Prognosis. Retrospective Studies. Risk Assessment. Survival Rate. Tomography, X-Ray Computed. Treatment Outcome. Young Adult
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.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
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[Cites]
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[ISSN]
1432-5195
[Journal-full-title]
International orthopaedics
[ISO-abbreviation]
Int Orthop
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
[Other-IDs]
NLM/ PMC2899057
62.
Toy PC, White JR, Scarborough MT, Enneking WF, Gibbs CP:
Distal femoral osteoarticular allografts: long-term survival, but frequent complications.
Clin Orthop Relat Res
; 2010 Nov;468(11):2914-23
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METHODS: We retrospectively reviewed 26 patients who had osteoarticular allograft reconstruction of the distal femur after resection of a malignant or aggressive
benign
tumor
of bone.
The 5-year and 10-year survival rates of the
joint
surface were 79% and 65%, respectively.
[MeSH-minor]
Adolescent. Adult. Amputation. Child. Female. Humans. Kaplan-Meier Estimate. Limb Salvage. Male. Middle Aged.
Neoplasm
Recurrence, Local / surgery.
Neoplasm
Staging. Recovery of Function. Reoperation. Retrospective Studies. Time Factors. Transplantation, Homologous. Treatment Outcome. Young Adult
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consumer health - Bone Grafts
.
COS Scholar Universe.
author profiles
.
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[
11398160.001
]
(PMID = 20645036.001).
[ISSN]
1528-1132
[Journal-full-title]
Clinical orthopaedics and related research
[ISO-abbreviation]
Clin. Orthop. Relat. Res.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2947705
63.
Ozcan C, Apaydin FD, Görür K, Apa DD:
Peripheral giant cell granuloma of the mandibular condyle presenting as a preauricular mass.
Eur Arch Otorhinolaryngol
; 2005 Mar;262(3):178-81
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Some rare extraparotid lesions, originating from the temporomandibular
joint
and the mandible itself, also share the same localization and therefore are to be taken into consideration for the differential
diagnosis
with parotid lesions.
Central GCG (CGCG) is an uncommon
benign
fibro-osseous lesion generally presenting as an expansible mass with cortical bone defect.
The brown
tumor
of hyperparathyroidism and giant cell
tumor
must be ruled out because of the microscopic similarities of these lesions.
The first case of PGCG of the mandible condyle is presented, and attention is drawn to mandibular diseases for the differential
diagnosis
of the preauricular mass.
[MeSH-minor]
Adult. Biopsy, Needle.
Diagnosis
, Differential. Female. Humans. Magnetic Resonance Imaging.
Neoplasm
Invasiveness. Tomography, X-Ray Computed
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[ISSN]
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[Journal-full-title]
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
[ISO-abbreviation]
Eur Arch Otorhinolaryngol
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
Germany
64.
Haque AU, Moatasim A:
Giant cell tumor of bone: a neoplasm or a reactive condition?
Int J Clin Exp Pathol
; 2008;1(6):489-501
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[Title]
Giant cell
tumor
of bone: a
neoplasm
or a reactive condition?
Giant cell
tumor
of bone (GCTB) is a
benign
but locally aggressive bone
tumor
of young adults.
Malignancy usually does not occur in GCTB and when discover, it usually represents primary bone sarcomas missed at original
diagnosis
.
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[ISSN]
1936-2625
[Journal-full-title]
International journal of clinical and experimental pathology
[ISO-abbreviation]
Int J Clin Exp Pathol
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2480584
[Keywords]
NOTNLM ; Giant cell tumor / aneurysmal bone cyst / bone / bone matrix / hemorrhage / osteoclast / osteoclastoma / telomerase
65.
Dominkus M, Ruggieri P, Bertoni F, Briccoli A, Picci P, Rocca M, Mercuri M:
Histologically verified lung metastases in benign giant cell tumours--14 cases from a single institution.
Int Orthop
; 2006 Dec;30(6):499-504
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[Title]
Histologically verified lung metastases in
benign
giant cell tumours--14 cases from a single institution.
From 1975 to 1997, 649 cases
of benign
giant cell tumours of the bone were treated at the Istituto Rizzoli.
The time interval between the
diagnosis
and the appearance of the lung metastases ranged from 3 months to 11.9 years.
In contrast to previous reports, we could not detect a predominance of the distal radius, but all of the patients had a stage III tumour according to the Enneking criteria
of benign
lesions.
We conclude that even metastatic
benign
giant cell tumours have an excellent prognosis after adequate resection.
[MeSH-major]
Bone Neoplasms / pathology. Giant Cell
Tumor
of Bone / secondary. Lung Neoplasms / secondary.
Neoplasm
Recurrence, Local / pathology
MedlinePlus Health Information.
consumer health - Bone Cancer
.
MedlinePlus Health Information.
consumer health - Lung Cancer
.
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Cancer. 1980 Oct 1;46(7):1641-9
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Cancer. 1984 Dec 1;54(11):2564-7
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]
(PMID = 16909252.001).
[ISSN]
0341-2695
[Journal-full-title]
International orthopaedics
[ISO-abbreviation]
Int Orthop
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Germany
[Other-IDs]
NLM/ PMC3172731
66.
Valdivielso-Ortiz A, Barber I, Soldado F, Aguirre-Canyadell M, Enriquez G:
Solitary osteochondroma: spontaneous regression.
Pediatr Radiol
; 2010 Oct;40(10):1699-701
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Osteochondromas are the most common
benign
bone tumours.
[MeSH-major]
Bone Neoplasms / diagnostic imaging. Femur / diagnostic imaging.
Neoplasm
Regression, Spontaneous. Osteochondroma / diagnostic imaging
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.
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[Cites]
Semin Roentgenol. 2005 Oct;40(4):380-90
[
16218554.001
]
[Cites]
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[
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[Cites]
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]
[Cites]
Radiographics. 2000 Sep-Oct;20(5):1407-34
[
10992031.001
]
(PMID = 20714716.001).
[ISSN]
1432-1998
[Journal-full-title]
Pediatric radiology
[ISO-abbreviation]
Pediatr Radiol
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
Germany
67.
Rehders A, Stoecklein NH, Poremba C, Alexander A, Knoefel WT, Peiper M:
Reexcision of soft tissue sarcoma: sufficient local control but increased rate of metastasis.
World J Surg
; 2009 Dec;33(12):2599-605
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BACKGROUND: Assuming a
benign
tumor
, soft tissue sarcomas are often treated by inadequate resection.
Therefore, it was our goal to evaluate the results of this treatment with particular respect to residual
tumor
.
The assessed endpoints were local recurrence-free survival, distant metastasis-free survival, and
tumor
-related mortality.
Residual
tumor
was detected in 43 patients (31%) and was significantly associated with reduced relapse-free and overall survival.
CONCLUSIONS: Despite an incomplete initial resection, reexcision enables local control similar to that in patients without residual
tumor
.
[MeSH-major]
Neoplasm
Recurrence, Local / surgery.
Neoplasm
, Residual / surgery. Sarcoma / surgery
[MeSH-minor]
Adolescent. Adult. Aged. Aged, 80 and over. Female. Humans. Male. Middle Aged.
Neoplasm
Metastasis. Reoperation. Survival Analysis. Young Adult
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[ErratumIn]
World J Surg. 2010 Aug;34(8):1991
[Cites]
Cancer. 2003 May 15;97(10):2544-53
[
12733154.001
]
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]
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[
16372156.001
]
(PMID = 19838751.001).
[ISSN]
1432-2323
[Journal-full-title]
World journal of surgery
[ISO-abbreviation]
World J Surg
[Language]
eng
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't
[Publication-country]
United States
68.
Nogueira Drumond JM:
EFFICACY OF THE ENNEKING STAGING SYSTEM IN RELATION TO TREATING BENIGN BONE TUMORS AND TUMOR-LIKE BONE LESIONS.
Rev Bras Ortop
; 2010 Jan;45(1):46-52
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[Title]
EFFICACY OF THE ENNEKING STAGING SYSTEM IN RELATION TO TREATING
BENIGN
BONE TUMORS AND
TUMOR
-LIKE BONE LESIONS.
OBJECTIVE: To evaluate the efficacy of the Enneking staging system for determining the prognosis, planning surgical treatment and indicating adjuvant therapy for
benign
bone tumors (BBT) and
tumor
-like bone lesions (TBL).
METHODS: A retrospective multicenter, descriptive, nonrandomized study was carried out on a representative sample comprising a large series of 165 patients with a total of 168
benign
bone tumors and
tumor
-like bone lesions.
Tumor
recurrence was significantly more frequent (p < 0.001) in the aggressive stage.
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(PMID = 27019838.001).
[ISSN]
2255-4971
[Journal-full-title]
Revista brasileira de ortopedia
[ISO-abbreviation]
Rev Bras Ortop
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Brazil
[Other-IDs]
NLM/ PMC4799048
[Keywords]
NOTNLM ; Bone diseases / Bone neoplasms/diagnosis/epidemiology/pathology/radiography/surgery / Neoplasm staging
69.
Zafatayeff-Hasbani S, Ducou Le Pointe H, Josset P, Damsin JP, Montagne JP:
Intra-articular recurrence of benign chondroblastoma with articular involvement at initial presentation--a case report.
Eur J Pediatr Surg
; 2006 Aug;16(4):291-3
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[Title]
Intra-articular recurrence
of benign
chondroblastoma with articular involvement at initial presentation--a case report.
[MeSH-minor]
Adolescent. Curettage. Epiphyses / pathology. Humans. Knee
Joint
. Male.
Neoplasm
Recurrence, Local.
Neoplasm
Seeding. Soft Tissue Neoplasms / pathology
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.
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consumer health - Bone Cancer
.
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(PMID = 16981100.001).
[ISSN]
0939-7248
[Journal-full-title]
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fuĢr Kinderchirurgie
[ISO-abbreviation]
Eur J Pediatr Surg
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
Germany
70.
Chamberlain AM, Anderson KL, Hoch B, Trumble TE, Weisstein JS:
Benign parosteal osteochondromatous proliferation of the hand originally diagnosed as osteochondroma: a report of two cases and review.
Hand (N Y)
; 2010 Mar;5(1):106-10
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[Title]
Benign
parosteal osteochondromatous proliferation of the hand originally diagnosed as osteochondroma: a report of two cases and review.
Bizarre parosteal osteochondromatous proliferation (BPOP) is a rare cartilaginous
neoplasm
that often presents in the long bones of the hands and feet.
BPOP is a
benign
but locally aggressive fibro-osseous mass that has striking clinical, radiographic, and histologic similarities with osteochondroma.
This report presents two cases of BPOP where initial clinical
diagnosis
of osteochondroma was made even after appropriate imaging and histologic samples were evaluated.
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[Cites]
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[ISSN]
1558-9455
[Journal-full-title]
Hand (New York, N.Y.)
[ISO-abbreviation]
Hand (N Y)
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
United States
[Other-IDs]
NLM/ PMC2820629
71.
Siƶsteen AK, Celsing F, Jacobsson H:
FDG uptake in a catheter-related thrombus simulating relapse of lymphoma.
Clin Nucl Med
; 2005 May;30(5):338-9
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There was an area of increased activity posterior to the left sternoclavicular
joint
, suspected of being a relapse.
Focal activity in relation to the tip of a venous catheter is very likely to have a
benign
etiology.
[MeSH-major]
Catheterization / adverse effects. Fluorodeoxyglucose F18 / pharmacokinetics. Lymphoma / metabolism. Lymphoma / radionuclide imaging.
Neoplasm
Recurrence, Local / radionuclide imaging. Venous Thrombosis / etiology. Venous Thrombosis / radionuclide imaging
[MeSH-minor]
Adolescent.
Diagnosis
, Differential. Humans. Male. Positron-Emission Tomography / methods. Radiopharmaceuticals / pharmacokinetics
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.
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(PMID = 15827407.001).
[ISSN]
0363-9762
[Journal-full-title]
Clinical nuclear medicine
[ISO-abbreviation]
Clin Nucl Med
[Language]
eng
[Publication-type]
Case Reports; Journal Article
[Publication-country]
United States
[Chemical-registry-number]
0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18
72.
Sohn SH, Koh SA, Kim DG, Park SW, Lee KH, Kim MK, Choi JH, Hyun MS:
A case of spine origin chondroblastoma metastasis to lung.
Cancer Res Treat
; 2009 Dec;41(4):241-4
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Chondroblastoma is a rare
benign
cartilaginous
neoplasm
that accounts for approximately 1% of all bone tumors and characteristically arises in the epiphysis of a long bone, particularly the humerus, tibia, and femur.
Unlike previously published examples of metastatic chondroblastoma, these metastasis developed before any operative manipulation of the primary
tumor
.
And primary
tumor
site was also unusual.
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[Cites]
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[ISSN]
2005-9256
[Journal-full-title]
Cancer research and treatment : official journal of Korean Cancer Association
[ISO-abbreviation]
Cancer Res Treat
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Korea (South)
[Other-IDs]
NLM/ PMC2802843
[Keywords]
NOTNLM ; Chondroblastoma / Lung metastasis / Spine origin
73.
Badar F, Moid I, Waheed F, Zaidi A, Naqvi B, Yunus S:
Variables associated with recurrence in breast cancer patients-the Shaukat Khanum Memorial experience.
Asian Pac J Cancer Prev
; 2005 Jan-Mar;6(1):54-7
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Those who presented with
benign
tumors, carcinoma in situ, or metastases were excluded from the analyses.
Age,
tumor
size, nodal status, menopause, estrogen receptor (ER), and progesterone receptor (PR) status, at the time of presentation, were determined.
Tumors were classified according to the TNM classification (American
Joint
Commission on Cancer (AJCC)-sixth edition), and subsequently, grouped into T1/T2 and T3/T4.
[MeSH-major]
Breast Neoplasms / pathology.
Neoplasm
Recurrence, Local
[MeSH-minor]
Adult. Aged. Aged, 80 and over. Chi-Square Distribution. Female. Follow-Up Studies. Humans. Logistic Models. Middle Aged.
Neoplasm
Metastasis.
Neoplasm
Staging. Pakistan / epidemiology. Registries. Risk Factors
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(PMID = 15780033.001).
[ISSN]
1513-7368
[Journal-full-title]
Asian Pacific journal of cancer prevention : APJCP
[ISO-abbreviation]
Asian Pac. J. Cancer Prev.
[Language]
eng
[Publication-type]
Journal Article
[Publication-country]
Thailand
74.
Fnini S, Labsaili N, Messoudi A, Largab A:
[Giant cell tumor of the thumb proximal phalanx: resection-iliac graft and double arthrodesis].
Chir Main
; 2008 Feb;27(1):54-7
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[Title]
[Giant cell
tumor
of the thumb proximal phalanx: resection-iliac graft and double arthrodesis].
Giant cell tumours (GCT) of bone are frequent, with variable behaviour, high risk of recurrence and an often
benign
histological appearance.
After a surgical biopsy, we performed an "en bloc" resection of the first phalanx, with an iliac crest graft reconstruction and a double arthrodesis of the metacarpophalangeal and interphalangeal
joint
.
[MeSH-major]
Bone Neoplasms. Giant Cell
Tumor
of Bone. Thumb
[MeSH-minor]
Arthrodesis. Biopsy. Bone Nails. Bone Transplantation. Finger
Joint
. Follow-Up Studies. Fracture Fixation, Internal / instrumentation. Fractures, Spontaneous / etiology. Fractures, Spontaneous / surgery. Humans. Male. Metacarpophalangeal
Joint
. Middle Aged.
Neoplasm
Staging. Patient Satisfaction. Time Factors. Treatment Outcome
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(PMID = 18248835.001).
[ISSN]
1297-3203
[Journal-full-title]
Chirurgie de la main
[ISO-abbreviation]
Chir Main
[Language]
fre
[Publication-type]
Case Reports; English Abstract; Journal Article
[Publication-country]
France
75.
Singh J, James SL, Kroon HM, Woertler K, Anderson SE, Jundt G, Davies AM:
Tumour and tumour-like lesions of the patella--a multicentre experience.
Eur Radiol
; 2009 Mar;19(3):701-12
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Of the 59 cases, 46% were non neoplastic, 39% were
benign
and 15% were malignant.
The commonest
benign neoplasm
was giant cell tumour (GCT) (11 cases).
Younger patients were more likely to have a
benign neoplasm
.
[MeSH-minor]
Adolescent. Adult. Age Factors.
Diagnosis
, Differential. Female. Humans. Male. Medical Oncology / methods. Middle Aged.
Neoplasm
Metastasis. Radiology / methods
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[ErratumIn]
Eur Radiol. 2010 Mar;20(3):763. Jundt, G [added]
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(PMID = 18815789.001).
[ISSN]
1432-1084
[Journal-full-title]
European radiology
[ISO-abbreviation]
Eur Radiol
[Language]
eng
[Publication-type]
Journal Article; Multicenter Study
[Publication-country]
Germany
76.
Zhang Y, Forootan SS, Liu D, Barraclough R, Foster CS, Rudland PS, Ke Y:
Increased expression of anterior gradient-2 is significantly associated with poor survival of prostate cancer patients.
Prostate Cancer Prostatic Dis
; 2007;10(3):293-300
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The relative levels of AGR2 expression in the malignant cell lines PC-3 and PC-3M were, respectively, 5.3+/-0.1 and 3.8+/-0.2 times that detected in the
benign
cell line PNT-2.
Amongst 34
benign
prostate hyperplastic (BPH) cases, 12 (35.3%) were unstained, 18 (52.9%) stained weakly positive and four (11.8%) stained moderately positive.
Increased
joint
Gleason score (GS) was significantly (log rank test, P=0.001) associated with poor patient survival.
[MeSH-major]
Adenocarcinoma / metabolism. Adenocarcinoma / mortality. Biomarkers,
Tumor
/ analysis. Prostatic Neoplasms / metabolism. Prostatic Neoplasms / mortality. Proteins / metabolism
[MeSH-minor]
Aged. Blotting, Western. Cell Line,
Tumor
. Gene Expression. Humans. Immunohistochemistry. Kaplan-Meier Estimate. Male.
Neoplasm
Staging. Prostate-Specific Antigen / blood
Genetic Alliance.
consumer health - Prostate cancer
.
MedlinePlus Health Information.
consumer health - Prostate Cancer
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTAC Assay Portal.
NCI CPTAC Assay Portal
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
NCI CPTC Antibody Characterization Program.
NCI CPTC Antibody Characterization Program
.
The Lens.
Cited by Patents in
.
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(PMID = 17457305.001).
[ISSN]
1365-7852
[Journal-full-title]
Prostate cancer and prostatic diseases
[ISO-abbreviation]
Prostate Cancer Prostatic Dis.
[Language]
eng
[Grant]
United Kingdom / Medical Research Council / / G0501019
[Publication-type]
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
[Publication-country]
England
[Chemical-registry-number]
0 / Biomarkers, Tumor; 0 / Proteins; EC 3.4.21.77 / Prostate-Specific Antigen; EC 5.3.4.1 / AGR2 protein, human
77.
Arbeitsgemeinschaft Knochentumoren, Becker WT, Dohle J, Bernd L, Braun A, Cserhati M, Enderle A, Hovy L, Matejovsky Z, Szendroi M, Trieb K, Tunn PU:
Local recurrence of giant cell tumor of bone after intralesional treatment with and without adjuvant therapy.
J Bone Joint Surg Am
; 2008 May;90(5):1060-7
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[Title]
Local recurrence of giant cell
tumor
of bone after intralesional treatment with and without adjuvant therapy.
BACKGROUND: The use of adjuvants after curettage has been well established for the treatment of giant cell
tumor
of bone.
The purpose of this study was to analyze the rates of recurrence following different types of treatment as well as the influence of various factors of
tumor
presentation on those rates.
METHODS: The data regarding
benign
giant cell tumors of the appendicular skeleton from ten bone
tumor
centers were evaluated.
The recurrence rates associated with the different treatment modalities were analyzed, and hazard ratios for a recurrence were calculated for multiple factors of
tumor
presentation.
The recurrence rate following curettage of a primary
tumor
without the use of adjuvants (55%) was higher than that following the same treatment of a recurrent
tumor
(39%) (p = 0.033).
CONCLUSIONS: Use of polymethylmethacrylate as an adjuvant significantly reduces the recurrence rate following intralesional treatment
of benign
giant cell tumors, and it appears to be the therapy of choice for primary as well as recurrent giant cell tumors of bone.
The significantly better results following treatment of recurrent tumors without adjuvants compared with the results of the same treatment of primary tumors were probably related to increased surgical thoroughness brought about by the surgeon's awareness of dealing with a riskier
tumor
.
[MeSH-major]
Bone Cements / therapeutic use. Bone Neoplasms / therapy. Giant Cell
Tumor
of Bone / therapy.
Neoplasm
Recurrence, Local / prevention & control. Polymethyl Methacrylate / therapeutic use
[MeSH-minor]
Antineoplastic Agents / administration & dosage. Cautery. Combined Modality Therapy. Curettage. Female. Humans. Kaplan-Meier Estimate. Male.
Neoplasm
, Residual / prevention & control. Phenol / administration & dosage. Proportional Hazards Models. Retrospective Studies
MedlinePlus Health Information.
consumer health - Bone Cancer
.
Hazardous Substances Data Bank.
PHENOL
.
Hazardous Substances Data Bank.
SODIUM PHENOLATE
.
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(PMID = 18451399.001).
[ISSN]
1535-1386
[Journal-full-title]
The Journal of bone and joint surgery. American volume
[ISO-abbreviation]
J Bone Joint Surg Am
[Language]
eng
[Publication-type]
Comparative Study; Journal Article; Multicenter Study
[Publication-country]
United States
[Chemical-registry-number]
0 / Antineoplastic Agents; 0 / Bone Cements; 339NCG44TV / Phenol; 9011-14-7 / Polymethyl Methacrylate
78.
Mangal N, Sharma VK, Verma N, Agarwal AK, Sharma SP, Aneja S:
Ultrasound guided fine needle aspiration cytology in the diagnosis of retroperitoneal masses: A study of 85 cases.
J Cytol
; 2009 Jul;26(3):97-101
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[Title]
Ultrasound guided fine needle aspiration cytology in the
diagnosis
of retroperitoneal masses: A study of 85 cases.
BACKGROUND: The
diagnosis
of retroperitoneal lesions is one of the most difficult areas in surgical pathology.
Fine needle aspiration cytology has shown promising role in establishing the
diagnosis
in this region.
OBJECTIVES: This study was undertaken to evaluate the reliability of ultrasonography (USG)-guided fine needle aspiration cytology (FNAC) in distinguishing between
benign
and malignant lesions in the retroperitoneum, and to correlate the
diagnosis
by cytology of retroperitoneal masses with the results obtained by histology.
In the kidney, the maximum number of cases were of renal cell carcinoma (12-38%), followed by Wilm's
tumor
(6-19%), pyonephrosis (5-16%), renal cyst (4), angiomyolipoma (2), cortical pseudotumor (2), and tuberculosis (1).
Among the 24 soft tissue tumors in the study, seven (29%) were malignant and 17 (71%) were
benign
(lipoma being the most common
benign neoplasm
).
CONCLUSIONS: USG-guided FNAC is an inexpensive, rapid, safe, and accurate procedure for the
diagnosis
of retroperitoneal masses.
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