"Pseudorheumatoid" nodules in children.

نویسندگان

  • J Pournaras
  • A A Gibson
چکیده

Subcutaneous nodules which are characterised by central fibrinoid necrosis, surrounded by histiocytes and fibroblasts are traditionally considered to be manifestations of rheumatoid arthritis or rheumatic fever. In recent years, however, cases in which such nodules appeared in otherwise healthy children have been reported. Beatty (1959) reported nine children, aged between eleven days and nine years, with isolated nodules located on the scalp, ulnar aspect of the forearm, palm and dorsum of the foot, who had no manifestations of rheumatic disease. He postulated that these lesions represented an unusual reaction to trauma. Draheim, Johnson and Helwig (1959) reported fifty-seven children between three and six years old with subcutaneous nodules. One patient developed rheumatic fever but none had rheumatoid arthritis. Twenty-five per cent gave a history of injury. They suggested a relationship between the nodules and allergy. Taranta (1962) described nodules in a six-year-old girl, histologically identical to those seen in rheumatic disease; he considered an altered reaction to trauma as a possible cause. Altman and Caffrey (1964) reported similar nodules in two children without systemic disease. Mesara, Brody and Oberman (1966) introduced the term “pseudorheumatoid”, referring to subcutaneous nodules histologically resembling rheumatoid nodules but without evidence of systemic disease; they published ten cases in children and two in adults. None of them had collagen disease or developed it during a period of observation of from one to seventeen years, but after excision seven showed recurrent nodular formations. The authors could not explain the etiology, nor could they differentiate the nodules with certainty from rheumatoid nodules,

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Orbital pseudorheumatoid nodule.

Pseudorheumatoid nodules are necrobiotic granulomas that are not associated with any systemic disease but that histopathologically mimic the granulomas of rheumatic fever, rheumatoid arthritis, and systemic lupus erythematosus [14] . Pseudorheumatoid nodules usually involve the skin of the extremities or scalp, but may occasionally involve the periocular area [5-7]. We report an unusual case of...

متن کامل

Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia

PURPOSE To present the case of a 14-year-old boy with clinical and radiographic features of pseudorheumatoid chondrodyspalsia with additional, potentially serious, cervical malformations. METHODS Detailed clinical and radiological examinations were undertaken with emphasis on the usefulness of 3D-CT scanning. RESULTS There was synchondrosis between the odontoid and the body of the axis and ...

متن کامل

Pseudoseptic pseudogout in progressive pseudorheumatoid arthritis of childhood.

Progressive pseudorheumatoid arthritis of childhood is an uncommon arthropathy of unknown aetiology, which is related to spondyloepiphyseal dysplasia tarda. Previous reports have noted the absence of joint inflammation in this disease. An adult is described here with this arthropathy, who developed episodic acute inflammatory arthritis that mimicked septic arthritis, but proved to be pseudogout...

متن کامل

Clinicoradiographic presentation of a girl with progressive pseudorheumatoid arthropathy.

We report the case of a girl-child who manifested the clinicoradiographic features of pseudorheumatoid arthritis. 3D-CT scan of the craniocervical junction showed distinctive features of dystopic type of os odontoideum. The report highlights the necessity to explore the craniocervical junction in patients with progressive pseudorheumatoid arthropathy.

متن کامل

Pathologic motion patterns in patients with progressive pseudorheumatoid arthropathy of childhood

Introduction Progressive pseudorheumatoid arthropathy of childhood (PPAC) is a specific subtype of spondyloepiphyseal dysplasie (SED) tarda. The skeletal disorder and is characterized by polyarthropathy of large and small joints. Typical signs are prominent epiphysis, progressive joint stiffness, muscle weakness and early fatigue [1]. Optimized physiotherapy is the only effective strategy to sl...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of bone and joint surgery. British volume

دوره 53 4  شماره 

صفحات  -

تاریخ انتشار 1971