Range: 0.3-6.5 cm Microscopic • Well circumscribed and lobulated • Mostly composed of mature hyaline cartilage • Variable amounts of calcification • Ossification common • Granulomatous inflammation in 15% of cases • Rare tumors with extensive xanthogranulomatous inflammation • Myxoid matrix common (myxochondroma) • Rare tumors with extensive stromal fibrosis (fibrochondroma) • Morphologic variant: Chondroblastoma-like chondroma Top Differential Diagnoses • Synovial chondromatosis • Tophaceous pseudogout • Tumoral calcinosis • Extraskeletal myxoid chondrosarcoma • Calcifying aponeurotic fibroma • Myxochondroid metaplasia of plantar foot • Cutaneous mixed tumor with chondroid metaplasia • Tenosynovial giant cell tumor CT Scan of Soft Tissue ChondromaSoft tissue chondroma typically occurs in the digits of the hands and feet. It presents as a painless, well-demarcated mineralized mass, as demonstrated in this CT of a dorsal index finger lesion. Note the peripheral distribution of mineralization . Lobular Architecture of ChondromaSoft tissue chondroma typically has a lobular architecture with islands of hyaline cartilage separated by fibrous bands . Matrix calcification and ossification are common. Cytological Features of ChondromaHigh-power micrograph illustrates typical cytological features of soft tissue chondroma. The chondrocytes are often arranged in clusters, situated in lacunar spaces within a pale blue hyaline matrix, and have uniform round nuclei and abundant eosinophilic cytoplasm. Rare binucleated cells can be seen . Mitoses are rare. Calcified Hyaline CartilageAreas of very dense calcification are common, illustrated by heavy basophilic staining of the cartilage matrix. TERMINOLOGY Synonyms • Extraskeletal chondroma • Chondroma of soft parts • Fibrochondroma • Osteochondroma • Myxochondroma • Chondroblastoma-like chondroma Definitions • Benign hyaline cartilage neoplasm of soft tissue with predilection for hands and feet ETIOLOGY/PATHOGENESIS Neoplasm With Genetic Abnormalities • Rearrangement of 12q13-15 • Trisomy 5 • Aberrations of chromosome 11 • HMGA2 abnormalities CLINICAL ISSUES Epidemiology • Incidence Uncommon – Exact incidence unknown • Age Median: 4th decade – Range: Infancy to 9th decade • Sex F = M Presentation • Painless mass • Most common in hands and feet (60-95%) Especially in fingers (40-50%) • Rare sites Proximal extremities, trunk, head and neck, oral cavity, ear, upper aerodigestive tract, dura/extradural, skin, fallopian tube Treatment • Simple surgical excision Prognosis • Low recurrence rate (15-20%) Recurrences controlled by reexcision • No reports of malignant degeneration IMAGING General Features • Best diagnostic clue Small, well-demarcated lesion Mineralized soft tissue mass Acral extremity • Location Hands and feet Often in vicinity of joint or tendon No intraarticular or subperiosteal localization by definition • Morphology Most are calcified or ossified Sometimes erode and deform underlying bone MACROSCOPIC General Features • Well demarcated and bosselated • Spherical or oval • Rubbery or hard • Sometimes soft, friable, gelatinous, or cystic Size • Median: 1.6 cm Range: 0.3-6.5 cm MICROSCOPIC Histologic Features • Well-circumscribed and lobulated subcutaneous tumor • Mostly composed of mature hyaline cartilage • Chondrocytes located in lacunae Arranged diffusely or in small clusters Some have enlarged nuclei and moderate pleomorphism Very low mitotic rate • Variable amounts of calcification Granular stippled calcification that surrounds chondrocytes in lace-like pattern Only gold members can continue reading. Log In or Register to continue Share this:Click to share on Twitter (Opens in new window)Click to share on Facebook (Opens in new window)Like this:Like Loading... Related Related posts: Squamous Cell Carcinoma In Situ (Bowen Disease) Porocarcinoma Multinucleate Cell Angiohistiocytoma Glomus Tumors Stay updated, free articles. Join our Telegram channel Join Tags: Diagnostic Pathology: Neoplastic Dermatopathology Apr 24, 2017 | Posted by admin in PATHOLOGY & LABORATORY MEDICINE | Comments Off on Soft Tissue Chondroma Full access? Get Clinical Tree
Range: 0.3-6.5 cm Microscopic • Well circumscribed and lobulated • Mostly composed of mature hyaline cartilage • Variable amounts of calcification • Ossification common • Granulomatous inflammation in 15% of cases • Rare tumors with extensive xanthogranulomatous inflammation • Myxoid matrix common (myxochondroma) • Rare tumors with extensive stromal fibrosis (fibrochondroma) • Morphologic variant: Chondroblastoma-like chondroma Top Differential Diagnoses • Synovial chondromatosis • Tophaceous pseudogout • Tumoral calcinosis • Extraskeletal myxoid chondrosarcoma • Calcifying aponeurotic fibroma • Myxochondroid metaplasia of plantar foot • Cutaneous mixed tumor with chondroid metaplasia • Tenosynovial giant cell tumor CT Scan of Soft Tissue ChondromaSoft tissue chondroma typically occurs in the digits of the hands and feet. It presents as a painless, well-demarcated mineralized mass, as demonstrated in this CT of a dorsal index finger lesion. Note the peripheral distribution of mineralization . Lobular Architecture of ChondromaSoft tissue chondroma typically has a lobular architecture with islands of hyaline cartilage separated by fibrous bands . Matrix calcification and ossification are common. Cytological Features of ChondromaHigh-power micrograph illustrates typical cytological features of soft tissue chondroma. The chondrocytes are often arranged in clusters, situated in lacunar spaces within a pale blue hyaline matrix, and have uniform round nuclei and abundant eosinophilic cytoplasm. Rare binucleated cells can be seen . Mitoses are rare. Calcified Hyaline CartilageAreas of very dense calcification are common, illustrated by heavy basophilic staining of the cartilage matrix. TERMINOLOGY Synonyms • Extraskeletal chondroma • Chondroma of soft parts • Fibrochondroma • Osteochondroma • Myxochondroma • Chondroblastoma-like chondroma Definitions • Benign hyaline cartilage neoplasm of soft tissue with predilection for hands and feet ETIOLOGY/PATHOGENESIS Neoplasm With Genetic Abnormalities • Rearrangement of 12q13-15 • Trisomy 5 • Aberrations of chromosome 11 • HMGA2 abnormalities CLINICAL ISSUES Epidemiology • Incidence Uncommon – Exact incidence unknown • Age Median: 4th decade – Range: Infancy to 9th decade • Sex F = M Presentation • Painless mass • Most common in hands and feet (60-95%) Especially in fingers (40-50%) • Rare sites Proximal extremities, trunk, head and neck, oral cavity, ear, upper aerodigestive tract, dura/extradural, skin, fallopian tube Treatment • Simple surgical excision Prognosis • Low recurrence rate (15-20%) Recurrences controlled by reexcision • No reports of malignant degeneration IMAGING General Features • Best diagnostic clue Small, well-demarcated lesion Mineralized soft tissue mass Acral extremity • Location Hands and feet Often in vicinity of joint or tendon No intraarticular or subperiosteal localization by definition • Morphology Most are calcified or ossified Sometimes erode and deform underlying bone MACROSCOPIC General Features • Well demarcated and bosselated • Spherical or oval • Rubbery or hard • Sometimes soft, friable, gelatinous, or cystic Size • Median: 1.6 cm Range: 0.3-6.5 cm MICROSCOPIC Histologic Features • Well-circumscribed and lobulated subcutaneous tumor • Mostly composed of mature hyaline cartilage • Chondrocytes located in lacunae Arranged diffusely or in small clusters Some have enlarged nuclei and moderate pleomorphism Very low mitotic rate • Variable amounts of calcification Granular stippled calcification that surrounds chondrocytes in lace-like pattern Only gold members can continue reading. Log In or Register to continue Share this:Click to share on Twitter (Opens in new window)Click to share on Facebook (Opens in new window)Like this:Like Loading... Related Related posts: Squamous Cell Carcinoma In Situ (Bowen Disease) Porocarcinoma Multinucleate Cell Angiohistiocytoma Glomus Tumors Stay updated, free articles. Join our Telegram channel Join Tags: Diagnostic Pathology: Neoplastic Dermatopathology Apr 24, 2017 | Posted by admin in PATHOLOGY & LABORATORY MEDICINE | Comments Off on Soft Tissue Chondroma Full access? Get Clinical Tree