RESUMO
We report the case of an 80-year-old woman who presented with an asymptomatic slowly growing mass in the dorsal aspect of her right wrist. Radiographs revealed a snail-shaped radiopaque structure. Surgical exploration and excision revealed a calcified lesion over the extensor digitorum communis. Histopathological analysis confirmed the diagnosis of tenosynovial chondromatosis. At the last follow-up, four years after surgery, the patient was asymptomatic and free of recurrence. Practitioners and hand surgeons should be aware of the dorsal involvement and evocative radiological calcifications of tenosynovial chondromatosis, which is a rare benign soft tissue neoplasm that affects all tendon sheaths of the hand.
Assuntos
Condromatose Sinovial , Condromatose , Neoplasias de Tecidos Moles , Humanos , Feminino , Idoso de 80 Anos ou mais , Punho , Condromatose/patologia , Condromatose Sinovial/diagnóstico por imagem , Condromatose Sinovial/cirurgia , Articulação do Punho/diagnóstico por imagem , Articulação do Punho/cirurgia , Neoplasias de Tecidos Moles/diagnóstico por imagem , Neoplasias de Tecidos Moles/cirurgia , Neoplasias de Tecidos Moles/patologiaRESUMO
This case report discusses a rare case of secondary tenosynovial chondromatosis of the flexor hallucis longus (FHL). Synovial chrondomatosis is a rare, benign proliferative cartilaginous lesion arising from the synovial tissue or bursal lining of or near joints. When it is extra-articular, it is considered tenosynovial chondromatosis. The diagnosis is often delayed given the rarity of presentation and non-specific symptoms. The case was highly unusual in that hindfoot pain was caused by several centimetre-sized osteochondral bodies within the FHL tendon sheath. Anterior cheilectomy was performed. The patient returned to full activity following surgery without recurrence of the disease. The condition can be successfully treated operatively.
Assuntos
Condromatose Sinovial , Condromatose , Humanos , Condromatose Sinovial/diagnóstico por imagem , Condromatose Sinovial/cirurgia , Condromatose/patologia , Imageamento por Ressonância Magnética , Tendões/cirurgia , Tendões/patologia , Músculo Esquelético/patologiaRESUMO
OBJECTIVE: To investigate the diagnosis and treatment procedure of synovial chondromatosis (SC) of the temporomandibular joint (TMJ). METHODS: Clinical features, imaging features, surgical methods, and prognosis of 7 patients with SC of the TMJ were analyzed. We also reviewed and analyzed surgery-relevant literature included in the Pubmed database in the past decade using the search terms "synovial chondromatosis" and "temporomandibular joint", and found 181 cases. RESULTS: There was no specific difference in the symptoms of SC in the TMJ in different Milgram's stages in our cases and the cases mentioned in the literature. The main symptoms of SC in the TMJ were pain (100%, 7/7; 64.64%, 117/181), limited mouth opening (57.14%, 4/7; 53.59%, 97/181), swelling (14.29%, 1/7; 28.18%, 51/181), crepitus (28.57%, 2/7; 19.34%, 35/181), and clicking (14.29%, 1/7; 9.94%, 18/181) in our cases and cases from literature separately. The imaging features of SC were occupying lesions (including loose bodies or masses) (71.42%, 5/7; 37.57%, 68/181), bone change in condyle or glenoid fossa (1/7, 14.29%; 34.81%, 63/181), effusion (42.86%, 3/7; 20.99%, 38/181), joint space changes (42.86%, 3/7; 11.05%, 20/181) in our cases and cases from literature separately. The surgical procedures seem to depend mainly on the involved structures and the extension of the lesion rather than the Milgram's stage. CONCLUSIONS: The clinical features of SC in the TMJ are nonspecific and easy to be misdiagnosed. MRI is helpful in the diagnosis of SC in the TMJ. The surgical procedures mainly depend on the involved structures and the extension of the lesion.
Assuntos
Condromatose Sinovial , Condromatose , Corpos Livres Articulares , Transtornos da Articulação Temporomandibular , Condromatose/patologia , Condromatose Sinovial/diagnóstico por imagem , Condromatose Sinovial/cirurgia , Humanos , Corpos Livres Articulares/patologia , Corpos Livres Articulares/cirurgia , Articulação Temporomandibular/diagnóstico por imagem , Articulação Temporomandibular/patologia , Articulação Temporomandibular/cirurgia , Transtornos da Articulação Temporomandibular/diagnóstico por imagem , Transtornos da Articulação Temporomandibular/cirurgiaRESUMO
Tenosynovial chondromatosis is a rare benign disorder characterized by formation of cartilaginous bodies within the synovia of the tendon sheaths. Most commonly present in the hands and feet. Clinical presentation and plain radiography can be inconclusive, which can lead to misclassification, most often confused as a chondroma of soft parts. In this case, we report the clinical, radiologic, and histology of a 59-year-old man who presented with a 1-year history of mass on the right fifth digit with limitation of motion secondary to this condition. Surgical excision revealed multiple cartilaginous nodules of varying size arising from the flexor tendon sheath. The diagnosis was confirmed postoperatively by surgical histopathology. The postoperative course of the patient was uncomplicated and has achieved an excellent functional recovery.
Assuntos
Condromatose Sinovial , Condromatose , Condromatose/complicações , Condromatose/patologia , Condromatose Sinovial/diagnóstico por imagem , Condromatose Sinovial/patologia , Condromatose Sinovial/cirurgia , Dedos/patologia , Humanos , Masculino , Pessoa de Meia-Idade , Radiografia , Tendões/diagnóstico por imagem , Tendões/patologia , Tendões/cirurgiaRESUMO
Approximately 9000 different phenotypes are known in medicine. The definition phenotype includes both manifest diseases as well as features without any disease value and the pure genetic disposition to develop a disease (e.g. tumors or complex diseases); however, most phenotypes are rare monogenic hereditary diseases. Approximately 6400 of these phenotypes have so far been elucidated by molecular genetics and are caused by mutations in 4064 different genes. Of all genetic diseases, an estimated one third are associated with skin symptoms. Genodermatoses are the phenotypes predominantly related to the skin, of which approximately 600 are familiar to dermatologists. The syndromes with scaling and keratosis include cornification disorders where the symptoms are not limited to the skin. They are associated with skin symptoms such as ichthyosis, erythroderma and palmoplantar keratoderma but show additional symptoms from other organ groups. The typical combination of symptoms may be unique to a syndrome and therefore seminal for the diagnosis.
Assuntos
Neoplasias Ósseas , Condromatose , Ictiose , Ceratodermia Palmar e Plantar , Ceratose , Mutação/genética , Síndromes Neoplásicas Hereditárias , Neoplasias Ósseas/genética , Neoplasias Ósseas/patologia , Condromatose/genética , Condromatose/patologia , Humanos , Ictiose/genética , Ictiose/patologia , Ceratodermia Palmar e Plantar/genética , Ceratodermia Palmar e Plantar/patologia , Ceratose/genética , Ceratose/patologia , Síndromes Neoplásicas Hereditárias/genética , Síndromes Neoplásicas Hereditárias/patologia , Pele , SíndromeRESUMO
Metachondromatosis which was first described in 1971 by Maroteaux is a rare genetic disease consisting of osteochondromas and enchondromas, caused by loss of function of the PTPN11 gene. It is distinct from other cartilaginous tumors such as multiple osteochondromas and hereditary multiple exostosis by the distribution and orientation of lesions, and pattern of inheritance. In Metachondromatosis osteochondromas typically occur in hands, feet, femur, and tibia while enchondromas commonly affect the pelvic bones and femurs. Both tumors are generally reported to regress in adulthood. To the best of our knowledge only one case of Chondrosarcoma has been reported, and our case is the second reported case of Chondrosarcoma in metachondromatosis.
Assuntos
Neoplasias Ósseas/patologia , Condromatose/patologia , Condrossarcoma/patologia , Exostose Múltipla Hereditária/patologia , Adulto , Pé , Mãos , Humanos , MasculinoRESUMO
El condrosarcoma es un tumor óseo maligno de origen cartilaginoso. Es el tercero en frecuencia de los tumores óseos malignos, solo superado por el mieloma múltiple y el osteosarcoma. El 75% son lesiones primarias y el 25% restante pertenecen a categorías especiales, entre las que se cuentan las variantes anatomopatológicas y las formas secundarias. Un condrosarcoma secundario es aquel que aparece en una lesión cartilaginosa benigna preexistente, entre las que se incluyen el osteocondroma solitario, la osteocondromatosis múltiple, el encondroma, las diferentes encondromatosis y la condromatosis sinovial primaria. La incidencia de la transformación maligna es muy variable en función del tipo de lesión. En este trabajo se discuten e ilustran las diferentes formas de condrosarcomas secundarios, poniendo un especial énfasis en los hallazgos radiológicos que deben alertar y que permiten al radiólogo tener un papel central en el diagnóstico, manejo y seguimiento de estos pacientes (AU)
Chondrosarcomas are malignant bone tumors originating in cartilage. Chondrosarcoma is the third most common malignant bone tumor after multiple myeloma and osteosarcoma. About 75% of chondrosarcomas are primary lesions. The remaining 25% belong to special categories such as histologic variants and secondary forms. A secondary chondrosarcoma is one that appears in a pre-existing benign chondral lesion; the different types of secondary chondrosarcomas include solitary osteochondroma, multiple osteochondromatosis, enchondroma, the different types of enchondromatosis, and primary synovial chondromatosis. The incidence of this malignant transformation varies widely in function of the type of lesion. In this article, we discuss and illustrate the different types of secondary chondrosarcomas, placing special emphasis on the imaging findings that should alert to these lesions and give radiologists a key role in the diagnosis, management, and follow-up of these patients (AU)
Assuntos
Adulto , Feminino , Humanos , Masculino , Condrossarcoma/patologia , Condrossarcoma , Osteocondroma/patologia , Osteocondroma , Tomografia Computadorizada Multidetectores/instrumentação , Tomografia Computadorizada Multidetectores/métodos , Tomografia Computadorizada Multidetectores , Condroma/patologia , Condroma , Condromatose/patologia , Imageamento por Ressonância Magnética/métodos , Espectroscopia de Ressonância Magnética/métodos , Tomografia , Condromatose , Encondromatose/patologia , EncondromatoseRESUMO
Genochondromatosis is an extremely rare autosomal dominant disorder, which manifests during childhood and tends to regress in adult life. The bony lesions are symmetrically distributed with characteristic localization at the metaphysis of proximal humerus and distal femur. Two types have been described based on the involvement of clavicle. Usually asymptomatic, sometimes patients may present with pathological fractures. In this communication, we describe four members of a family with Genochondromatosis type I, with some additional clinical and radiological findings not reported previously.
Assuntos
Neoplasias Ósseas/diagnóstico por imagem , Neoplasias Ósseas/patologia , Condromatose/diagnóstico por imagem , Condromatose/patologia , Síndromes Neoplásicas Hereditárias/diagnóstico por imagem , Síndromes Neoplásicas Hereditárias/patologia , Adolescente , Adulto , Criança , Diagnóstico Diferencial , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Linhagem , Radiografia , Rádio (Anatomia)/patologiaRESUMO
Loss of PTPN11/SHP2 in mice or in human metachondromatosis (MC) patients causes benign cartilage tumors on the bone surface (exostoses) and within bones (enchondromas). To elucidate the mechanisms underlying cartilage tumor formation, we investigated the role of SHP2 in the specification, maturation and organization of chondrocytes. Firstly, we studied chondrocyte maturation by performing RNA-seq on primary chondrocyte pellet cultures. We found that SHP2 depletion, or inhibition of the ERK1/2 pathway, delays the terminal differentiation of chondrocytes from the early-hypertrophic to the late-hypertrophic stage. Secondly, we studied chondrocyte maturation and organization in mice with a mosaic postnatal inactivation of Ptpn11 in chondrocytes. We found that the vertebral growth plates of these mice have expanded domains of early-hypertrophic chondrocytes that have not yet terminally differentiated, and their enchondroma-like lesions arise from chondrocytes displaced from the growth plate due to a disruption in the organization of maturation and ossification zones. Furthermore, we observed that lesions from human MC patients also display disorganized chondrocyte maturation zones. Next, we found that inactivation of Ptpn11 in Fsp1-Cre-expressing fibroblasts induces exostosis-like outgrowths, suggesting that loss of SHP2 in cells on the bone surface and at bone-ligament attachment sites induces ectopic chondrogenesis. Finally, we performed lineage tracing to show that exostoses and enchondromas in mice likely contain mixtures of wild-type and SHP2-deficient chondrocytes. Together, these data indicate that in patients with MC, who are heterozygous for inherited PTPN11 loss-of-function mutations, second-hit mutations in PTPN11 can induce enchondromas by disrupting the organization and delaying the terminal differentiation of growth plate chondrocytes, and can induce exostoses by causing ectopic chondrogenesis of cells on the bone surface. Furthermore, the data are consistent with paracrine signaling from SHP2-deficient cells causing SHP2-sufficient cells to be incorporated into the lesions.
Assuntos
Cartilagem/metabolismo , Diferenciação Celular/genética , Comunicação Parácrina/genética , Proteína Tirosina Fosfatase não Receptora Tipo 11/genética , Animais , Neoplasias Ósseas/genética , Neoplasias Ósseas/patologia , Cartilagem/patologia , Condrócitos/metabolismo , Condrócitos/patologia , Condrogênese/genética , Condroma/genética , Condroma/patologia , Condromatose/genética , Condromatose/patologia , Exostose/genética , Exostose/patologia , Exostose Múltipla Hereditária/genética , Exostose Múltipla Hereditária/patologia , Lâmina de Crescimento , Humanos , Sistema de Sinalização das MAP Quinases/genética , Camundongos , Osteogênese/genética , Proteína Tirosina Fosfatase não Receptora Tipo 11/metabolismoRESUMO
Metachondromatosis is a benign bone disease predominantly observed in the hands and feet of children or young adults demonstrating two different manifestations: a cartilage-capped bony outgrowth on the surface of the bone called exostosis and ectopic cartilaginous nodules inside the bone called enchondroma. Recently, it has been reported that loss-of-function mutations of the SHP2 gene, which encodes the SHP2 protein tyrosine phosphatase, are associated with metachondromatosis. The purpose of this study was to investigate the role of SHP2 in postnatal cartilage development, which is largely unknown. We disrupted Shp2 during the postnatal stage of mouse development in a chondrocyte-specific manner using a tamoxifen-inducible system. We found tumor-like nodules on the hands and feet within a month after the initial induction. The SHP2-deficient mice demonstrated an exostosis-like and enchondroma-like phenotype in multiple bones of the hands, feet, and ribs as assessed by X-ray and micro-computed tomography (CT). Histological assessment revealed the disorganization of the growth plate cartilage, a cartilaginous protrusion from the epiphyseal bone, and ectopic cartilage nodules within the bones, which is consistent with the pathological features of metachondromatosis in humans (ie, both exostosis and enchondroma). At molecular levels, we observed an abundant expression of Indian hedgehog protein (IHH) and fibroblast growth factor 2 (FGF2) and impaired expression of mitogen-activated protein kinases (MAPK) in the affected cartilage nodules in the SHP2-deficient mice. In summary, we have generated a mouse model of metachondromatosis that includes manifestations of exostosis and enchondroma. This study provides a novel model for the investigation of the pathophysiology of the disease and advances the understanding of metachondromatosis. This model will be useful to identify molecular mechanisms for the disease cause and progression as well as to develop new therapeutic strategies in the future.
Assuntos
Neoplasias Ósseas/patologia , Cartilagem/metabolismo , Condrócitos/citologia , Condromatose/patologia , Exostose Múltipla Hereditária/patologia , Domínios de Homologia de src/genética , Animais , Neoplasias Ósseas/metabolismo , Condrócitos/metabolismo , Condromatose/metabolismo , Exostose Múltipla Hereditária/metabolismo , Sistema de Sinalização das MAP Quinases , Camundongos , Camundongos Knockout , Reação em Cadeia da Polimerase em Tempo Real , Transdução de SinaisAssuntos
Neoplasias Ósseas/metabolismo , Neoplasias Ósseas/patologia , Condromatose/metabolismo , Condromatose/patologia , Exostose Múltipla Hereditária/metabolismo , Exostose Múltipla Hereditária/patologia , Proteínas Hedgehog/metabolismo , Células-Tronco Mesenquimais/metabolismo , Proteína Tirosina Fosfatase não Receptora Tipo 11/deficiência , Transdução de Sinais , AnimaisRESUMO
The tyrosine phosphatase SHP2, encoded by PTPN11, is required for the survival, proliferation and differentiation of various cell types. Germline activating mutations in PTPN11 cause Noonan syndrome, whereas somatic PTPN11 mutations cause childhood myeloproliferative disease and contribute to some solid tumours. Recently, heterozygous inactivating mutations in PTPN11 were found in metachondromatosis, a rare inherited disorder featuring multiple exostoses, enchondromas, joint destruction and bony deformities. The detailed pathogenesis of this disorder has remained unclear. Here we use a conditional knockout (floxed) Ptpn11 allele (Ptpn11(fl)) and Cre recombinase transgenic mice to delete Ptpn11 specifically in monocytes, macrophages and osteoclasts (lysozyme M-Cre; LysMCre) or in cathepsin K (Ctsk)-expressing cells, previously thought to be osteoclasts. LysMCre;Ptpn11(fl/fl) mice had mild osteopetrosis. Notably, however, CtskCre;Ptpn11(fl/fl) mice developed features very similar to metachondromatosis. Lineage tracing revealed a novel population of CtskCre-expressing cells in the perichondrial groove of Ranvier that display markers and functional properties consistent with mesenchymal progenitors. Chondroid neoplasms arise from these cells and show decreased extracellular signal-regulated kinase (ERK) pathway activation, increased Indian hedgehog (Ihh) and parathyroid hormone-related protein (Pthrp, also known as Pthlh) expression and excessive proliferation. Shp2-deficient chondroprogenitors had decreased fibroblast growth factor-evoked ERK activation and enhanced Ihh and Pthrp expression, whereas fibroblast growth factor receptor (FGFR) or mitogen-activated protein kinase kinase (MEK) inhibitor treatment of chondroid cells increased Ihh and Pthrp expression. Importantly, smoothened inhibitor treatment ameliorated metachondromatosis features in CtskCre;Ptpn11(fl/fl) mice. Thus, in contrast to its pro-oncogenic role in haematopoietic and epithelial cells, Ptpn11 is a tumour suppressor in cartilage, acting through a FGFR/MEK/ERK-dependent pathway in a novel progenitor cell population to prevent excessive Ihh production.
Assuntos
Neoplasias Ósseas/metabolismo , Neoplasias Ósseas/patologia , Condromatose/metabolismo , Condromatose/patologia , Exostose Múltipla Hereditária/metabolismo , Exostose Múltipla Hereditária/patologia , Proteínas Hedgehog/metabolismo , Células-Tronco Mesenquimais/metabolismo , Proteína Tirosina Fosfatase não Receptora Tipo 11/deficiência , Transdução de Sinais , Animais , Neoplasias Ósseas/tratamento farmacológico , Neoplasias Ósseas/genética , Cartilagem/metabolismo , Cartilagem/patologia , Catepsina K/deficiência , Catepsina K/genética , Catepsina K/metabolismo , Divisão Celular , Linhagem da Célula , Condromatose/tratamento farmacológico , Condromatose/genética , Exostose Múltipla Hereditária/tratamento farmacológico , Exostose Múltipla Hereditária/genética , Fatores de Crescimento de Fibroblastos/metabolismo , Deleção de Genes , Regulação da Expressão Gênica/efeitos dos fármacos , Genes Supressores de Tumor/fisiologia , Proteínas Hedgehog/antagonistas & inibidores , Sistema de Sinalização das MAP Quinases , Macrófagos/metabolismo , Células-Tronco Mesenquimais/citologia , Camundongos , Camundongos Knockout , Camundongos Transgênicos , Quinases de Proteína Quinase Ativadas por Mitógeno/antagonistas & inibidores , Quinases de Proteína Quinase Ativadas por Mitógeno/metabolismo , Monócitos/metabolismo , Osteoclastos/metabolismo , Osteopetrose/genética , Osteopetrose/metabolismo , Osteopetrose/patologia , Proteína Relacionada ao Hormônio Paratireóideo/metabolismo , Proteína Tirosina Fosfatase não Receptora Tipo 11/genética , Proteína Tirosina Fosfatase não Receptora Tipo 11/metabolismo , Transdução de Sinais/efeitos dos fármacosRESUMO
Laryngeal chondromas are uncommon, benign, slow-growing neoplasms with few reports in the literature. Vocal fold chondromas are even more rare, and all reported cases are unilateral. Here, we present the first case of bilateral vocal fold chondromas. Detailed evaluation, careful resection with phonomicrosurgery technique, and perioperative voice therapy are considered essential for the management.
Assuntos
Condromatose , Neoplasias Laríngeas , Prega Vocal , Condromatose/patologia , Condromatose/fisiopatologia , Condromatose/cirurgia , Humanos , Neoplasias Laríngeas/patologia , Neoplasias Laríngeas/fisiopatologia , Neoplasias Laríngeas/cirurgia , Laringoscopia/métodos , Masculino , Microcirurgia , Pessoa de Meia-Idade , Fonação , Valor Preditivo dos Testes , Procedimentos de Cirurgia Plástica , Recuperação de Função Fisiológica , Resultado do Tratamento , Prega Vocal/patologia , Prega Vocal/fisiopatologia , Prega Vocal/cirurgia , Qualidade da Voz , Treinamento da VozRESUMO
We used exome sequencing of blood DNA in four unrelated patients to identify the genetic basis of metaphyseal chondromatosis with urinary excretion of D-2-hydroxy-glutaric acid (MC-HGA), a rare entity comprising severe chondrodysplasia, organic aciduria, and variable cerebral involvement. No evidence for recessive mutations was found; instead, two patients showed mutations in IDH1 predicting p.R132H and p.R132S as apparent somatic mosaicism. Sanger sequencing confirmed the presence of the mutation in blood DNA in one patient, and in blood and saliva (but not in fibroblast) DNA in the other patient. Mutations at codon 132 of IDH1 change the enzymatic specificity of the cytoplasmic isocitrate dehydrogenase enzyme. They result in increased D-2-hydroxy-glutarate production, α-ketoglutarate depletion, activation of HIF-1α (a key regulator of chondrocyte proliferation at the growth plate), and reduction of N-acetyl-aspartyl-glutamate level in glial cells. Thus, somatic mutations in IDH1 may explain all features of MC-HGA, including sporadic occurrence, metaphyseal disorganization, and chondromatosis, urinary excretion of D-2-hydroxy-glutaric acid, and reduced cerebral myelinization.
Assuntos
Encefalopatias Metabólicas Congênitas/genética , Condromatose/genética , Isocitrato Desidrogenase/genética , Encefalopatias Metabólicas Congênitas/sangue , Encefalopatias Metabólicas Congênitas/enzimologia , Encefalopatias Metabólicas Congênitas/patologia , Encefalopatias Metabólicas Congênitas/urina , Condromatose/sangue , Condromatose/enzimologia , Condromatose/patologia , Análise Mutacional de DNA/métodos , Exoma , Feminino , Estudos de Associação Genética/métodos , Genoma Humano , Genótipo , Glutaratos/urina , Humanos , Subunidade alfa do Fator 1 Induzível por Hipóxia/metabolismo , Lactente , Isocitrato Desidrogenase/sangue , Ácidos Cetoglutáricos/metabolismo , Masculino , Mutação , Saliva/química , Especificidade por SubstratoAssuntos
Neoplasias Ósseas/classificação , Ameloblastoma/patologia , Neoplasias Ósseas/genética , Neoplasias Ósseas/patologia , Condromatose/patologia , Condrossarcoma/classificação , Condrossarcoma/patologia , Encondromatose/patologia , Humanos , Osteossarcoma/classificação , Osteossarcoma/patologia , Sarcoma de Ewing/patologia , Sociedades Médicas , Estados Unidos , Organização Mundial da SaúdeRESUMO
Intra- and extra-articular primary synovial chondromatosis (SC) was observed in a five-year-old, entire male German Shepherd. Thousands of small cartilaginous nodules were removed from the stifle joint as well as from several adjacent muscles. Diagnosis of SC was established based on clinical, radiographic and biopsy results. The owner declined to have a new surgery performed for complete nodule removal and partial synovectomy. Nine months after the initial presentation, a proximal pathological intra- articular tibial fracture was observed and malignant transformation to chondrosarcoma was diagnosed after limb amputation. No metastasis was observed after 1.5 years of follow-up.
Assuntos
Condromatose Sinovial/patologia , Condromatose/patologia , Condrossarcoma/veterinária , Amputação Cirúrgica/veterinária , Animais , Transformação Celular Neoplásica/patologia , Condrócitos/patologia , Condromatose/diagnóstico por imagem , Condromatose/veterinária , Condromatose Sinovial/diagnóstico por imagem , Condromatose Sinovial/veterinária , Condrossarcoma/patologia , Condrossarcoma/cirurgia , Cães , Coxeadura Animal/etiologia , Coxeadura Animal/patologia , Masculino , Radiografia , Joelho de Quadrúpedes/diagnóstico por imagem , Joelho de Quadrúpedes/patologia , Membrana Sinovial/patologiaAssuntos
Condromatose/diagnóstico , Fibroma/diagnóstico , Neoplasias Mandibulares/diagnóstico , Glândula Parótida/patologia , Adenoma/diagnóstico , Biópsia por Agulha Fina , Condromatose/patologia , Diagnóstico Diferencial , Feminino , Fibroma/patologia , Humanos , Neoplasias Mandibulares/patologia , Pessoa de Meia-Idade , Invasividade Neoplásica , Neoplasias Parotídeas/diagnóstico , Neoplasias das Glândulas Salivares/diagnósticoRESUMO
OBJECTIVE: To evaluate cell cultures derived from intrasynovial nodules from a patient with primary synovial chondromatosis (PSC) for aberrant numbers/differentiation of osteochondroprogenitor cells. METHODS: Cell cultures were established from PSC synovial nodules, or normal bovine or human osteoarthritis (OA) synovia (for comparison). Multi-lineage potential was determined using well-characterized in vitro culture systems to assess osteogenic, chondrogenic and adipogenic capability. RESULTS: Primary PSC cell cultures were typically fibroblastic but contained islands of dense cell clusters/nodules, some of which were isolated and cultured separately [putative osteochondroprogenitris (pOCP) cultures]. OA synovial cultures had barely detectable levels of alkaline phosphatase (AP) that increased (0.006+/-0.008 to 0.141+/-0.000 nmol p-nitrophenol/min/cm(2)) with dexamethasone treatment. AP activity was higher in primary PSC cell cultures and further enhanced by dexamethasone (from 0.076+/-0.022 to 5.735+/-0.000 nmol p-nitrophenol/min/cm(2)). Histochemically, AP was localized as discreet areas within PSC cultures. No AP activity was detected histochemically in OA or normal bovine synovial cultures. The pOCP cultures had high basal AP (5.036+/-0.439 nmol p-nitrophenol/min/cm(2)) and spontaneously formed mineralized nodules, which increased in number under standard osteogenic conditions. Under chondrogenic conditions, micromass or pellet-cultured pOCP cells spontaneously synthesized a matrix containing glycosaminoglycans and collagen II. In adipogenic medium, the number of lipid-containing cells was increased. CONCLUSIONS: Compared with cultures established from OA or normal synovia, cell cultures established from PSC synovial nodules were enriched in osteochondroprogenitors, which, unlike normal mesenchymal cells, differentiated along chondrogenic and osteogenic lineages in the absence of dexamethasone.
Assuntos
Condromatose/patologia , Células-Tronco/patologia , Líquido Sinovial/citologia , Adulto , Idoso , Fosfatase Alcalina/metabolismo , Animais , Bovinos , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células , Células Cultivadas , Condrogênese , Dexametasona/farmacologia , Feminino , Glucocorticoides/farmacologia , Humanos , Masculino , Osteoartrite do Joelho/patologia , Osteogênese/efeitos dos fármacos , Células-Tronco/efeitos dos fármacos , Células-Tronco/enzimologia , Líquido Sinovial/efeitos dos fármacos , Líquido Sinovial/enzimologiaAssuntos
Condromatose/patologia , Neoplasias de Tecidos Moles/patologia , Neoplasias de Tecidos Moles/cirurgia , Membrana Sinovial/patologia , Articulação do Tornozelo/patologia , Articulação do Tornozelo/cirurgia , Biópsia por Agulha , Criança , Condromatose/cirurgia , Seguimentos , Humanos , Imuno-Histoquímica , Imageamento por Ressonância Magnética/métodos , Masculino , Dor , Medição de Risco , Sinovectomia , Resultado do TratamentoRESUMO
A 41 year old man with a history of politrauma presented with a nodular mass of the left false vocal cord, associated with progressive dysphonia, dyspnoea, and dysphagia. A computed tomography scan of the neck region showed a rounded and circumscribed mass without infiltration of the surrounding tissues. Histological investigation of the nodule revealed the presence of fibroelastic cartilaginous tissue, surrounded by a thin rim of fibrous tissue, with rare hypercellular areas, occasional binucleated cells, slight hyperchromasia, and an irregular nuclear profile. Mitotic activity was absent. The patient's history of laryngeal trauma, with the subsequent progressive onset of clinical symptoms, helps to distinguish the chondrometaplastic nature of this nodule from true laryngeal cartilaginous tumours, such as chondroma and low grade chondrosarcoma.