Tumors of the bones of the feet: the clinicopathologic features of 150 cases

Bakotic, Bradley W.; Huvos, Andrew G.

doi:10.1016/s1067-2516(01)80063-6

Cited by 65 publications

(42 citation statements)

References 21 publications

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“…Bony tumors of the hindfoot are rare with limited literature available [1,5,16,19,23]. Delay in diagnosis or missed diagnosis of hindfoot lesions is frequently reported [2,6,7,9,10,15,22].…”

Section: Discussionmentioning

confidence: 99%

“…The talus was a rare location accounting for just 8% of benign lesions and none that were malignant [16]. The existing literature is limited: there have been two location-specific small case series of calcaneus and talus, respectively [4,10], three case series of osseous neoplasms of the foot [1,5,16] or the hand and foot [19], and tumor-specific review articles [3,7,8,11,13,17,18,21]. The majority comprise individual case reports describing specific osseous lesions and their treatment.…”

Section: Introductionmentioning

confidence: 99%

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Primary Osseous Tumors of the Hindfoot: Why the Delay in Diagnosis and Should We Be Concerned?

Young

Bell

MacDuff

et al. 2013

Clinical Orthopaedics &Amp; Related Research

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Background Bony tumors of the foot account for approximately 3% of all osseous tumors. Diagnosis is frequently delayed as a result of lack of clinician familiarity and as a result of their rarity. The reasons for the delays, however, are unclear. Questions/purposes We therefore determined (1) how hindfoot tumors present and the specific reasons for delay in diagnosis; (2) whether the spectrum of disease varies between the talus and calcaneus; and (3) how these patients were treated. Methods We retrospectively reviewed the medical notes and imaging for all patients with 34 calcaneal and 23 talar tumors recorded in the Scottish Bone Tumour Registry. Demographics, presentation, investigation, histology, management, recurrence, and mortality were recorded.

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Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Primary Osseous Tumors of the Hindfoot: Why the Delay in Diagnosis and Should We Be Concerned?

Young

Bell

MacDuff

et al. 2013

Clinical Orthopaedics &Amp; Related Research

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“…Leeson et al, dans une série de 827 tumeurs primitives, rapportent une fréquence de 1,7 % [2]. Sur 150 tumeurs osseuses du pied analysées par Bakotic et Huvos [3], dix étaient des métastases. Pour certains auteurs, ces acrométastases du pied sembleraient être encore plus rares qu'au niveau de la main [4,5].…”

Section: Discussionunclassified

“…Le diagnostic différentiel se fait principalement avec la goutte [3,6,9,11,12], une infection ostéoarticulaire et la maladie de Paget [8].…”

Section: Discussionunclassified

Acrométastase du pied révélant un cancer bronchique: à propos d’un cas

et al. 2010

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L'acrométastase osseuse du pied comme manifestation initiale révélatrice d'une tumeur maligne primitive occulte est exceptionnellement rapportée dans la littérature. Les retards, voire les erreurs diagnostiques, sont fréquents. Nous rapportons un cas d'acrométastase au niveau de la tête du premier métatarsien révélant un adénocarcinome pulmonaire. Mots clés Acrométastase · Pied · Premier métatarsien · Adénocarcinome pulmonaireAbstract Foot bone acrometastasis, as the first manifestation of an occult primary malignant tumor, is rarely reported in the literature, and delayed or inappropriate diagnosis is frequent. We report a case of arcometastasis at the head of the first metatarsus revealing an occult lung adenocarcinoma.

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“…This tumor needs to be diVerentiated from malignant tumors, such as chondrosarcoma, clear cell chondrosarcoma and osteosarcoma; and from other benign lesions such as enchondroma, giant cell tumor, chondromyxoid Wbroma, aneurysmal bone cyst, and osteoblastoma [2,11,12,15]. Generally, chondroblastoma is composed of medium-sized, round or multinucleated cells with a distinct border, and the giant cells generally have several to more than ten small nuclei.…”

Section: Discussionmentioning

confidence: 99%

A case of pathological fracture associated with chondroblastoma of the first metatarsal: natural development over 3 years

Kobayashi

Takeno

Uchida

et al. 2008

Eur J Orthop Surg Traumatol

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Chondroblastoma of the metatarsal is a very rare condition. To our knowledge fewer than 20 cases have been reported in the world literature. We report a 34-yearold man with chondroblastoma of the Wrst metatarsal. The clinical, radiological and pathological aspects of the tumor are discussed. On pathological examination, there were no typical Wndings suggestive of benign chondroblastoma such as chicken wire calciWcation. Therefore, it was diYcult to determine whether the eosinophilic matrix observed in the stroma was osteoid or cartilaginous tissue, and diVerentiation from osteoblastoma was needed. However, the followup period of this patient was prolonged, and pain that was possibly due to pathologic fracture had occurred during this period, suggesting that these factors could have promoted Wbrosis. The patient was treated by curettage and autologous bone grafting. At 4 years after surgery, there has been no evidence of recurrent tumor.

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Tumors of the bones of the feet: the clinicopathologic features of 150 cases

Cited by 65 publications

References 21 publications

Primary Osseous Tumors of the Hindfoot: Why the Delay in Diagnosis and Should We Be Concerned?

Primary Osseous Tumors of the Hindfoot: Why the Delay in Diagnosis and Should We Be Concerned?

Acrométastase du pied révélant un cancer bronchique: à propos d’un cas

A case of pathological fracture associated with chondroblastoma of the first metatarsal: natural development over 3 years

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