The History of Paediatrics: The Progress of the Study of Diseases of Children up to the End of the XVIIIth Century, by George Frederic Still, M.D. London: Dawsons of Pall Mall, 1965, 526 pp., 5.10.0 ($15.50)

PEDIATRICS ◽  
1966 ◽  
Vol 37 (6) ◽  
pp. 920-920
Author(s):  
Samuel X. Radbill

First published in 1931 as an enlargement upon the Fitzpatrick lectures which were given a few years earlier at the Royal College of Physicians in London, the original edition of this book had become a rarity thanks to Hitler's bombers which destroyed all but about 800 copies. Now this facsimile reprint will meet an eager welcome. It complements Ruhräh's Pediatrics of the Past, which Still, in his preface, described as so "masterly and delightful an anthology." Using the biographical method, the growth of medical interest in children is traced chronologically from Hippocrates to Jenner, a period from about 400 B.C. to 1800 A.D. An appendix listing pediatric inaugural dissertations written between the years 1573 and 1799 and another listing minor writings, dissertations, and pamphlets from 1729 to 1797, as well as an index of names and subjects, add to the usefulness of the book. George Frederic Still (1868-1941), whose last name is the eponym for juvenile rheumatoid arthritis (the theme of his graduation thesis in 1897), was one of the first in England to devote himself to pediatrics as a modem specialty. He was the first professor of diseases of children in King's College, London, and the author of many important pediatric papers, as well as several books among which is his popular and beautifully written textbook on Common Disorders and Diseases of Children. But his most enduring gift to mankind is this remarkably accurate and scholarly study of the history of pediatrics. This reprint is a photocopy of the original. Nothing but the name of the publisher on the title page has been altered, which will prove a boon to true scholars even though it stops short of the nineteenth and twentieth cunturies.

1923 ◽  
Vol 2 (4) ◽  
pp. 783-804
Author(s):  
E. Denison Ross

Since the appearance of the last number of this Bulletin I have had the good fortune to find the outer cover of the King's College manuscript of Almeida's History of Ethiopia, which had hitherto been missing. The discovery is important, for attached to this cover there was not only the original title page, but also the “Preliminary Matter” referred to by Marsden in his Catalogue, occupying in all eleven folios. The contents are as follows:—


2020 ◽  
pp. 83-88
Author(s):  
A.B. Volosyanko ◽  
◽  
M.I. Reitmeyer ◽  
L.Ya. Ivanyshyn ◽  
◽  
...  

1962 ◽  
Vol 1 (3) ◽  
pp. 148-151
Author(s):  
Andrew M. Margileth

1. Our experience with a six-year-old boy who had diarrhea, urethritis, conjunctivitis and arthritis is presented as a classical case of Reiter's syndrome. The patient recovered fully in a period of five months and has remained well during the past five years. 2. The cause of Reiter's syndrome remains unknown but in children may be related to Flexner bacillus dysentery. 3. The disease in children is usually less severe than in adults and all 11 children reported have recovered. The recent literature is reviewed. 4. Treatment with antibiotics is of no value and steroid therapy has not prevented exacerbations nor shortened the course of the disease. 5. The nongonococcal triad of urethritis, conjunctivitis, and arthritis is a distinct clinicopathologic entity which differs from known infections and juvenile rheumatoid arthritis.


PEDIATRICS ◽  
1984 ◽  
Vol 73 (3) ◽  
pp. 400-400

It is well recognized that a paralyzed limb may be spared from the effects of joint disease in patients with rheumatoid arthritis (RA),1 osteoarthritis,2,3 and gout.4 The paralysis may result from upper or lower motor neuron lesions.5-7 The striking freedom from lower extremity joint involvement in a child with polyarticular juvenile rheumatoid arthritis (JRA) represents a further example of this association, the first reported in a child. CASE REPORT An 8½-year-old girl had a 2-year history of pain in the metacarpophalangeal joints, hands, neck, and shoulders. She had noted decreased upper limb strength, inability to extend her elbows fully, and a recent diminution of range of motion in her wrists and shoulders.


Author(s):  
R Fundora ◽  
S Juman ◽  
C Felix ◽  
J Clarke

A Bezold abscess is a rare complication of acute otitis media and mastoiditis which is characterized by the collection of pus in the sub-muscular spaces from the mastoid cavity. A 27-year-old female with history of Juvenile Rheumatoid Arthritis presented with right ear discharge and post auricular swelling extending along the sternocleidomastoid muscle. A Bezold abscess was diagnosed upon review of the patient’s CT scan. She subsequently underwent incision and drainage of the abscess in addition to a cortical mastoidectomy. Although the development of intra and extra axial complications of acute otitis media are very rare in the post antibiotic and vaccination era, it should be noted that a compromised immune system is a significant risk factor for this complication.


PEDIATRICS ◽  
1993 ◽  
Vol 92 (2) ◽  
pp. 295-296
Author(s):  

Chronic, nongranulomatous iridocyclitis is an important complication of juvenile rheumatoid arthritis (JRA).1-3 First reported by Ohm in 1910, the association between iridocycitis and JRA has become well established. The intraocular inflammation referred to as iridocyclitis primarily affects the iris and ciliary body. Overall, the reported incidence of iridocyditis varies from 2% to 21% in children with JRA.4 The morbidity of iridocydlitis includes cataracts, glaucoma, band keratopathy, and loss of vision.5,6 Diagnosis of early iridocycitis is usually not possible by routine direct ophthalmoscopy. Sitlamp examination detects the signs of active anterior chamber inflammation. Guidelines for the schedule of routine serial sitlamp examination are suggested for early detection of iridocycitis. The presentation of eye involvement in JRA may be asymptomatic or of an insidious onset. The outcome has improved in the past 20 years. The majority of children have a relatively good visual prognosis if the iridocycitis is detected and treated early.6 RISK FACTORS FOR IRIDOCYCLITIS Articular Features The diagnosis of JRA describes a heterogeneous group of arthritic conditions with onset of disease before age 16 years. There are three major subtypes of JRA: systemic onset, polyarticular onset, and pauciarticular onset, defined by the clinical manifestations in the first 6 weeks of the disease.7 Fewer than 2% of children with systemic-onset JRA have iridocycitis.4,5 Children with polyarticular disease are at moderate risk, with 7% to 37% incidence of iridocyditis. The majority of children with iridocycitis have pauciarticular disease.1-3,5 The onset of the iridocyclitis may precede the onset of the arthritis in approximately 6% of cases.


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