RESUMO
Intracranial xanthogranulomas (XGs) have been found at various sites, but xanthogranuloma of the sellar region is extremely rare. We report about a case of sellar XG in a 34-year-old female. Magnetic resonance imaging showed a solid-cystic mass located at the sella turcica. The cystic component was hyperintense on the T1-weighted image (WI) and T2WI. The solid component was hyperintense on T1WI and hypointense on T2WI. There was peripheral enhancement after gadolinium administration. The diagnosis of cystic macroadenoma was considered before surgery. Final diagnosis of XG was confirmed by histopathological examination after surgical resection. Gross total resection of the lesion was achieved using the microscope through endoscopic endonasal transsphenoidal approach. The patient had a good outcome and no symptom of diabetes insipidus, hormonal evaluation did not show any alterations compatible with hypopituitarism and prolactin levels were normal XG should receive diagnostic consideration for the sellar mass lesions with cystic components hyperintense on T1WI and T2WI, solid components hyperintense on T1WI and hypointense on T2WI, and CT without evidence of calcifications. It is important to consider the possibility of XG when pertinent, as it facilitates a proper surgical approach strategy.
Assuntos
Neoplasias Hipofisárias , Xantomatose , Feminino , Humanos , Adulto , Imageamento por Ressonância Magnética , Sela Túrcica/diagnóstico por imagem , Sela Túrcica/cirurgia , Sela Túrcica/patologia , Endoscopia , Granuloma/patologia , Xantomatose/diagnóstico por imagem , Xantomatose/cirurgia , Xantomatose/patologia , Neoplasias Hipofisárias/diagnóstico por imagem , Neoplasias Hipofisárias/cirurgiaRESUMO
OBJETIVO Presentación de un inusual caso de xantomatosis cerebrotendinosa en un paciente de edad cuya primera manifestación fueron xantomas bilaterales del tendón de Aquiles. MATERIAL Y MÉTODOS Mujer de 62 años, que presenta tumoraciones, que presenta tumoraciones sólidas y polilobuladas, en la cara posterior de ambos tendones de Aquiles de 8 años de evolución. El diagnóstico se realizó mediante el hallazgo de hiperlipidemia y estudio genético. Se realió la exóresis quirúrgica parcial de las tumoraciones. RESULTADOS A los 5 años de la cirugía del pie izquierdo y 4 años del pie derecho la paciente estaba asintomática. Presentaba una fuerza para la flexión plantar bilateral de 5/5, pudiendo caminar y subir escaleras sin molestias. Presentaba una escala AOFAS de 85 y 90 puntos en el pie izquierdo y derecho, respectivamente. No hubo recidivas. DISCUSIÓN Los xantomas son depósitos de colesterol en el tejido conectivo de la piel, tendones o fascia, como resultado de una hiperlipoproteinemia. La importancia del caso radica en su sospecha diagnóstica, ya que la xantomatosis cerebrotendinosa suele manifestarse en pacientes de menos de 30 años de edad y en los que se ha recomendado la resección radical de las tumoraciones, e incluso del tendón, debido a las frecuentes recidivas. CONCLUSIÓN En pacientes de mayor edad con lesiones que infiltran el tendón, se puede optar por un tratamiento menos agresivo con un buen resultado clínico.
OBJETIVE Presentation of an unusual case of cerebrotendinous xanthomatosis in an elderly patient whose first manifestation was bilateral Achilles tendon xanthomas. MATERIAL AND METHODS 62-year-old woman presenting solid and polylobed tumors on the posterior aspect of both Achilles tendons for eight years. The diagnosis was made by means of hyperlipidemia and a genetic study. Surgical partial excision of the tumors was performed. RESULTS Five years after surgery on the left foot and four years after the right foot, the patient was asymptomatic. Bilateral plantar flexion force was 5/5, The patient was able to walk and climb stairs without discomfort. AOFAS score was 85 and 90 on the left and right feet, respectively. There were no recurrences. DISCUSSION Xanthomatosis is a genetic alteration with deposits of cholesterol in connective tissue of the skin, tendons or fascia, because of hyperlipoproteinemia. The importance of the present case lies in its diagnostic suspicion, since cerebrotendinous xanthomatosis manifests usually in patients under 30 years of age and in whom radical resection of tumors, and even of the tendon, has been recommended due to frequent recurrences . CONCLUSION In older patients with tumors that infiltrate the tendon, a less aggressive treatment can be chosen with a good clinical result.
Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Tendão do Calcâneo , Xantomatose/cirurgia , Xantomatose/diagnóstico , Xantomatose Cerebrotendinosa/complicações , Tendinopatia/cirurgia , Tendinopatia/diagnóstico , Imageamento por Ressonância Magnética , Xantomatose/etiologia , Xantomatose/diagnóstico por imagem , Tendinopatia/etiologia , Tendinopatia/diagnóstico por imagem , HiperlipidemiasRESUMO
A 32-year-old man presented to the dermatology department with generalized asymptomatic yellowish papules on an erythematous base, arms, thighs, and buttocks. These lesions had appeared in the previous month (Figure 1). Dermoscopy revealed a homogeneous yellow color, corresponding to dermal xanthomatous deposits, with interconnected fine and dotted vessels (Figure 2). The laboratory findings showed extremely high levels of triglycerides (4.842 mg/dL; normal <150), as well as increased total cholesterol (576 mg/dL; normal <200), fasting blood glucose (294 mg/dL), and glycated hemoglobin 12.3% (normal range 4% to 6%). A skin biopsy demonstrated foamy cells, with extracellular lipid between collagen bundles in the dermis (Figure 3).
Assuntos
Complicações do Diabetes/complicações , Hipertrigliceridemia/etiologia , Xantomatose/etiologia , Xantomatose/patologia , Adulto , Biópsia , Dermoscopia , Complicações do Diabetes/diagnóstico , Humanos , Masculino , Pele/patologia , Xantomatose/diagnóstico por imagemRESUMO
BACKGROUND AND AIMS: Achilles tendon xanthomas (ATX) are a sign of long-term exposure to high blood cholesterol in familial hypercholesterolemia (FH) patients, which have been associated with cardiovascular disease. We evaluated the ATX association with the presence and extent of subclinical coronary atherosclerosis in heterozygous FH patients. METHODS: 102 FH patients diagnosed by US-MEDPED criteria (67% with genetically proven FH), with median LDL-C 279 mg/dL (interquartile range: 240; 313), asymptomatic for cardiovascular disease, underwent computed tomography angiography and coronary artery calcium (CAC) quantification. Subclinical coronary atherosclerosis was quantified by CAC, segment-stenosis (SSS) and segment-involvement (SIS) scores. Adjusted Poisson regression was used to assess the association of ATX with subclinical atherosclerosis burden as continuous variables. RESULTS: Patients with ATX (n = 21, 21%) had higher LDL-C and lipoprotein(a) [Lp(a)] concentrations as well as greater CAC scores, SIS and SSS (p < 0.05). After adjusting for age, sex, smoking, hypertension, previous statin use, HDL-C, LDL-C and Lp(a) concentrations, there was an independent positive association of ATX presence with CAC scores (ß = 1.017, p < 0.001), SSS (ß = 0.809, p < 0.001) and SIS (ß = 0.640, p < 0.001). CONCLUSIONS: ATX are independently associated with the extension of subclinical coronary atherosclerosis quantified by tomographic scores in FH patients.
Assuntos
Tendão do Calcâneo , Apolipoproteína B-100/genética , Doença da Artéria Coronariana/etiologia , Heterozigoto , Hiperlipoproteinemia Tipo II/genética , Mutação , Receptores de LDL/genética , Xantomatose/etiologia , Tendão do Calcâneo/diagnóstico por imagem , Adulto , Doenças Assintomáticas , Biomarcadores/sangue , HDL-Colesterol/sangue , LDL-Colesterol/sangue , Angiografia por Tomografia Computadorizada , Angiografia Coronária/métodos , Doença da Artéria Coronariana/diagnóstico por imagem , Estudos Transversais , Feminino , Predisposição Genética para Doença , Humanos , Hiperlipoproteinemia Tipo II/sangue , Hiperlipoproteinemia Tipo II/complicações , Hiperlipoproteinemia Tipo II/diagnóstico , Lipoproteína(a)/sangue , Masculino , Pessoa de Meia-Idade , Fenótipo , Projetos Piloto , Índice de Gravidade de Doença , Xantomatose/diagnóstico por imagemRESUMO
Xanthomatous lesions of the sellar region have traditionally been divided into two separate categories, xanthomatous hypophysitis (XH) and xanthogranuloma (XG) of the sellar region. The seminal article on XH, a condition typified by foamy histiocytes and lymphoplasmacytic infiltrates in the pituitary gland/sellar region, but usually little or no hemosiderin pigment, detailed three patients. However, most reports since that time have been single cases, making understanding of the entity difficult. In contrast, the seminal report on XG, characterized by sellar region cholesterol clefts, lymphoplasmacytic infiltrates, marked hemosiderin deposits, fibrosis, multinucleated giant cells around cholesterol clefts, eosinophilic granular necrotic debris, and accumulation of macrophages, included 37 patients, allowing more insights into etiology. Few examples could be linked to adamantinomatous craniopharyngioma, and although ciliated epithelium similar to that of Rathke cleft cyst (RCC) was identified up to 35% of the 37 cases, it could not be proven that XG was related to hemorrhage into RCC. Case reports since that time, however, occasionally linked XG to RCC when an etiology could be identified at all, and a few recognized that a spectrum exists in xanthomatous lesions of the sella. They review literature, adding 23 cases from our own experience, to confirm that overlap occurs between XH and XG, and that the majority-but not all-can be linked to RCC leakage/rupture/hemorrhage. It was suggested that progressive accumulation of hemosiderin pigment in the lesion, possibly caused by the multiple episodes of bleeding, could account for the transition of at least some cases of XH to XG.
Assuntos
Doenças da Hipófise/epidemiologia , Doenças da Hipófise/patologia , Sela Túrcica , Xantomatose/epidemiologia , Xantomatose/patologia , Adolescente , Adulto , Idoso , Encéfalo/diagnóstico por imagem , Criança , Pré-Escolar , Estudos de Coortes , Feminino , Granuloma/diagnóstico por imagem , Granuloma/epidemiologia , Granuloma/patologia , Granuloma/terapia , Humanos , Hipofisite , Masculino , Pessoa de Meia-Idade , Doenças da Hipófise/diagnóstico por imagem , Doenças da Hipófise/terapia , Xantomatose/diagnóstico por imagem , Xantomatose/terapia , Adulto JovemRESUMO
O xantoma no tendão calcâneo é uma doença rara e tem uma alta associação com hiperlipidemia primária. O diagnóstico precoce é fundamental para o início do tratamento e para alterar o curso da doença. Os exames de imagem podem auxiliar nesse diagnóstico. Este estudo relata o caso de um homem de 60 anos apresentando nódulos indolores nos cotovelos e tendões calcâneos, sem crises típicas de gota, acompanhado no ambulatório de doenças microcristalinas da Unifesp para esclarecimento diagnóstico. Os testes laboratoriais solicitados apresentavam dislipidemia. Ultrassom (US) mostrou espessamento difuso dos tendões calcâneos com áreas hipoecoicas. Ressonância magnética (RM) mostrou espessamento difuso dos tendões, com áreas de sinal intermediário e padrão reticulado no interior. Os exames de imagem mostraram aspectos relevantes no diagnóstico de xantoma, auxiliando no diagnóstico diferencial.
The Achilles tendon xanthoma is a rare disease and has a high association with primary hyperlipidemia. An early diagnosis is essential to start treatment and change the disease course. Imaging exams can enhance diagnosis. This study reports the case of a 60-year-old man having painless nodules on his elbows and Achilles tendons without typical gout crisis, followed in the microcrystalline disease clinic of Unifesp for diagnostic workup. Laboratory tests obtained showed dyslipidemia. The ultrasound (US) showed a diffuse Achilles tendon thickening with hypoechoic areas. Magnetic resonance imaging (MRI) showed a diffuse tendon thickening with intermediate signal areas, and a reticulate pattern within. Imaging studies showed relevant aspects to diagnose a xanthoma, thus helping in the differential diagnosis.
Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Tendão do Calcâneo , Imageamento por Ressonância Magnética , Ultrassonografia , Xantomatose/diagnóstico por imagem , TendinopatiaRESUMO
The Achilles tendon xanthoma is a rare disease and has a high association with primary hyperlipidemia. An early diagnosis is essential to start treatment and change the disease course. Imaging exams can enhance diagnosis. This study reports the case of a 60-year-old man having painless nodules on his elbows and Achilles tendons without typical gout crisis, followed in the microcrystalline disease clinic of Unifesp for diagnostic workup. Laboratory tests obtained showed dyslipidemia. The ultrasound (US) showed a diffuse Achilles tendon thickening with hypoechoic areas. Magnetic resonance imaging (MRI) showed a diffuse tendon thickening with intermediate signal areas, and a reticulate pattern within. Imaging studies showed relevant aspects to diagnose a xanthoma, thus helping in the differential diagnosis.
Assuntos
Tendão do Calcâneo , Imageamento por Ressonância Magnética , Ultrassonografia , Xantomatose/diagnóstico por imagem , Humanos , Masculino , Pessoa de Meia-Idade , TendinopatiaRESUMO
El xantoma intraóseo (XIO) es un tumor óseo benigno extremadamente raro. En la histología se caracteriza por presentar macrófagos mononucleares, abundantes células espumosas y células gigantes multinucleadas. Puede aparecer asociado a otras enfermedades (XIO secundario), principalmente a desórdenes lipídicos, o en forma aislada (XIO primario). Los XIO son lesiones líticas expansivas que a menudo se encuentran en pacientes con condiciones hiperlipidémicas. En la mayoría de los casos la evaluación inicial se realiza con radiografía, aunque otros procedimientos pueden ser necesarios para confirmar el diagnóstico. Se presenta el caso de un hombre de 48 años que consultó por lumbalgia con irradiación al miembro inferior derecho e impotencia funcional de 3 meses de evolución. Tenía hallazgos imagenológicos de XIO en el hueso ilíaco derecho, sin hiperlipidemia o lesiones preexistentes. Se llevó a cabo la extirpación total del tumor y el posterior estudio histopatológico de la pieza operatoria confirmó el diagnóstico. El tratamiento resultó exitoso. El objetivo de este artículo es describir los hallazgos clínicos e imagenológicos (radiografía, resonancia magnética, tomografía computada y medicina nuclear) de un XIO primario y su tratamiento. Además, realizamos una breve revisión de la literatura.
Abstract Intraosseous xanthoma is an extremely rare benign bone tumor. Histology shows mononuclear macrophages, abundant foam cells and multinucleated giant cells. The intraosseous xanthoma may appear associated with other diseases (secondary intraosseous xanthoma), mainly lipid disorders or without an underlying lipid disorder (primary intraosseous xanthoma). The intraosseous xanthoma is a lytic, expansive tumor, often seen in patients with hyperlipidemic conditions. In most cases, the initial evaluation is performed with X-ray, although other procedures may be necessary to confirm the diagnosis. We report the case of a man aged 48, who consulted for back pain radiating to the right leg and functional disability 3 months duration, with imaging findings in the right iliac XIO in the absence of pre-existing injuries or hyperlipidemic conditions, so surgery for total removal of the tumor was performed with histological examination of the surgical specimen, confirming the preoperative diagnosis of XIO. Such treatment resulted curative. The aim of this article is to describe the clinical, imaging findings (RX, MRI, CT, nuclear medicine) and the course of treatment of a committing the iliac primary intraosseous xanthoma a and a normolipidemic patient brief review of the literature.
Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias Ósseas/diagnóstico por imagem , Xantomatose/diagnóstico por imagem , Pelve/diagnóstico por imagem , Radiografia , Tomografia Computadorizada por Raios X , Células Espumosas/patologia , Quadril/diagnóstico por imagemRESUMO
Bone xanthomas are rare and are usually are associated with endocrine or metabolic diseases, mainly lipid disorders. In the absence of systemic diseases, the lesion is called a primary xanthoma. Primary mandibular xanthomas are extremely rare. The aim of this report is to describe the clinical and radiographic findings of a primary mandibular xanthoma, discussing the epidemiological features, pathogenesis and differential diagnosis. A 25-year-old man was referred for evaluation of a left mandibular lesion detected in a routine radiographic exam. Radiographically, there was a diffuse, unilocular and radiolucent lesion, with irregular margins located adjacent to the surface from the distal root of the left mandibular third molar. The lesion was excised under local anaesthesia. Microscopically, there were several cells with a foamy and granular cytoplasm and central small, round nuclei, similar to xanthomatous macrophages. No lipid disorders were diagnosed. According to these features, the diagnosis of primary mandibular xanthoma was established. In conclusion, xanthomas of the jaws are rare and all seem to be primary and occur exclusively in the mandible.