Imaging features of osteoid osteoma of the phalanges

Kotnis, Nikhil; James, Steven

doi:10.1007/s00256-015-2191-8

Cited by 8 publications

(11 citation statements)

References 26 publications

(49 reference statements)

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“…Metabolic disease: Gaucher disease. Bone disease: osteofibrous disease, osteoid osteoma [94][95][96][97][98]. Neoplastic: Langerhans cell histiocytoma, leukemia-associated osteoarthralgia, sarcoma [99,100].…”

Section: Pathogenic Bme In Childrenmentioning

confidence: 99%

How We Manage Bone Marrow Edema—An Interdisciplinary Approach

Baumbach

Pfahler

Pozza

et al. 2020

JCM

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Bone marrow edema (BME) is a descriptive term for a common finding in magnetic resonance imaging (MRI). Although pain is the major symptom, BME differs in terms of its causal mechanisms, underlying disease, as well as treatment and prognosis. This complexity together with the lack of evidence-based guidelines, frequently makes the identification of underlying conditions and its management a major challenge. Unnecessary multiple consultations and delays in diagnosis as well as therapy indicate a need for interdisciplinary clinical recommendations. Therefore, an interdisciplinary task force was set up within our large osteology center consisting of specialists from internal medicine, endocrinology/diabetology, hematology/oncology, orthopedics, pediatrics, physical medicine, radiology, rheumatology, and trauma surgery to develop a consenus paper. After review of literature, review of practical experiences (expert opinion), and determination of consensus findings, an overview and an algorithm were developed with concise summaries of relevant aspects of the respective underlying disease including diagnostic measures, clinical features, differential diagnosis and treatment of BME. Together, our single-center consensus review on the management of BME may help improve the quality of care for these patients.

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Section: Pathogenic Bme In Childrenmentioning

confidence: 99%

How We Manage Bone Marrow Edema—An Interdisciplinary Approach

Baumbach

Pfahler

Pozza

et al. 2020

JCM

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“…1,4,20,21,23,25–27 However, any age is possible ranging from reports of congenital OO 28 to 1 case of a 70-year-old male being affected. 21 Although OO in general is frequently cited as being 2 to 3 times more common in males, 1,25 the average of 10 large case series over the last 30 years shows a more equivalent sex ratio of 1.3:1 (male:female) for OO cases in the hand and wrist.…”

Section: Discussionmentioning

confidence: 99%

“…21 Although OO in general is frequently cited as being 2 to 3 times more common in males, 1,25 the average of 10 large case series over the last 30 years shows a more equivalent sex ratio of 1.3:1 (male:female) for OO cases in the hand and wrist. 1,3,4,11,20,21,25–27,29 Based on the data available, the right hand appears to be involved 1.9 times more frequently than the left. 1,3,4,20,21 …”

Section: Discussionmentioning

confidence: 99%

“…1,4,11,20,25,27 A more reliable modality is 99m Tc scintigraphy, which can diagnose OO in 91% of cases on average, 1,4,11,21 but may lack specificity due to diffuse isotope uptake in surrounding tissues. 1 MRI and CT imaging are successful in recognizing OO in all cases, though CT imaging was used 41% more often.…”

Section: Discussionmentioning

confidence: 99%

“…1 MRI and CT imaging are successful in recognizing OO in all cases, though CT imaging was used 41% more often. 1,4,11,27 CT is considered the most specific imaging modality for identifying OO, given the sensitivity of MRI for registering soft-tissue reaction surrounding the nidus that may confuse the diagnosis. 30 Of course, histology is the definitive diagnosis for all cases of OO in the hands and wrist.…”

Section: Discussionmentioning

confidence: 99%

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Proximal Phalanx Osteoid Osteoma: A Case Report and Literature Review

Liu

Stone

Alowami

et al. 2017

Plastic and Reconstructive Surgery - Global Open

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Summary:Osteoid osteoma is a rare clinical entity often mistaken for osteomyelitis, enchondroma, osteochondroma and other bony pathologies. Cardinal features include localized swelling and nocturnal pain often relieved by nonsteroidal antiinflammatory drugs. Definitive treatment requires surgical removal of the lesion by curettage or en bloc excision. The following case report details the diagnosis and management of a recurrent case of osteoid osteoma in a long finger proximal phalanx. Included with this case report is a literature review of osteoid osteomas on the hand and the anatomic distribution of 289 cases published in the last 30 years.

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