experimental myasthenia gravis

1
803 the working mother ? You state that "at 40 women are ready to go back to work "; but at that time a woman’s parents and those of her husband begin to fail and to need help, her husband may want more comfort, and soon the married daughters will require assistance. Do not tell me that these tasks should be taken over by the social-security personnel-a district nurse for half an hour and a home help for one hour a day are very poor substitutes for a daughter, a wife, or a mother in case of illness. Again, you say that " Only 20% of doctors in Britain (compared with 75% in U.S.S.R.) are women "; but it is clearly misleading to select as a model this single feature of an authoritarian system where everything is closely interconnected. The statistics of this country should be considered, which show how many of the girls who study Medicine, never practise. The policy of some medical schools of limiting the number of girl entrants should be judged from this angle. If, as you believe desirable, working women in all trades and professions come to make the best possible use of their abilities, the women of the future will have an institu- tionalised childhood and an institutionalised old age, and in between a working-life of rush, and nerve-racking strain, trying to fit two full-time professions into a 16-hours working dav. RAHEL LIEBESCHUETZ. EXPERIMENTAL MYASTHENIA GRAVIS Sir have followed with interest the work on the attempted production of myasthenia gravis in animals by injecting them with thymic or muscle extract in Freund’s complete adjuvant. Dr. Vetters and his colleagues (July 5, p. 28), who were unable to demonstrate the production of an experimental myasthenia, raise an important point which Dr. Kalden and Dr. Irvine (Sept. 20, p.638) have failed to answer. Vetters et al. question the validity of the thymitis, which, as I understand it, is essential for the production of the experimental disease. The thymitis is diagnosed histologic- ally by observing a dense aggregation of lymphocytes around Hassall’s corpuscles in the medulla. Goldstein et al. have described these findings in several papers.I-4 I submit that what is described as thymitis is in fact a 1. Goldstein, G., Whittingham, S. Lancet, 1966, ii, 315. 2. Goldstein, G., Whittingham, S. Clin. exp. Immunol. 1967, 2, 257. 3. Oppenheim, T. J., Goldstein, G. Nature, Lond. 1969, 222, 192. 4. Goldstein, G., Strauss, A. J. L., Pickeral, S. Clin. exp. Immunol. 1969, 4, 3. Fig. 1-Normal guineapig thymus with prominent aggregation of lymphocytes around Hassall’s corpuscles in the medulla. (Hsematoxylin and eosin; x 100.) Fig. 2-Higher-power view of medulla showing cuff of lympho- cytes around Hassall’s corpuscle. (Haematoxylin and eosin; x 225.) normal finding, which I have observed on many occasions in the thymus gland of normal outbred guineapigs (figs. 1 and 2). These illustrations are representative of many other normal thymus glands. They are almost identical to fig. 2b in Goldstein’s recent paper,4 which is said to show thymitis. I do not feel competent to judge the validity of the electromyographic data, but I would suggest that what Goldstein and his associates, and Kalden and Irvine, call a thymitis may be seen in the thymus of normal guineapigs. It would be unfortunate if a crucial pathological role was ascribed to the thymus in this experimental system, upon the demonstration of a histological appearance which can be readily observed in the normal guineapig thymus. J. N. WEBB. University Department of Pathology, Edinburgh. TREATMENT OF TETANUS SIR,-The modern treatment of tetanus outlined by Dr. Cole and Dr. Youngman 5 is too expensive to be adopted in developing countries where the disease is a major problem. The following is an analysis of the tetanus cases admitted during the 2-year period between Sept., 1967, and Aug., 1969, to the children’s department of this hospital, classified as of grade 2-3 severity by the criteria of Cole and Youngman. Apart from general nursing care, antibiotics, and atten- tion to local hygiene and nutrition, the standard manage- ment of these has been with chlorpromazine (2-4 mg. per kg.) given intramuscularly together with paraldehyde (0-2 ml. per kg.), and 50,000 units of tetanus antitoxin intra- muscularly 15-20 minutes after the chlorpromazine and paraldehyde. We have encountered no allergic reactions when this order has been carefully adopted. 3 further daily doses of 5000 units of antitoxin were given after admission. Spasms were controlled with diazepam (’ Valium ’), 1-2 mg. every 4-6 hours alternating with intramuscular paraldehyde until 48 hours after cessation. 5. Cole, L., Youngman, H. Lancet, 1969, i, 1017.

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Page 1: EXPERIMENTAL MYASTHENIA GRAVIS

803

the working mother ? You state that "at 40 women areready to go back to work "; but at that time a woman’sparents and those of her husband begin to fail and to needhelp, her husband may want more comfort, and soon themarried daughters will require assistance. Do not tell methat these tasks should be taken over by the social-securitypersonnel-a district nurse for half an hour and a home helpfor one hour a day are very poor substitutes for a daughter, awife, or a mother in case of illness. Again, you say that" Only 20% of doctors in Britain (compared with 75% inU.S.S.R.) are women "; but it is clearly misleading to selectas a model this single feature of an authoritarian systemwhere everything is closely interconnected. The statisticsof this country should be considered, which show how manyof the girls who study Medicine, never practise. The policyof some medical schools of limiting the number of girlentrants should be judged from this angle.

If, as you believe desirable, working women in all tradesand professions come to make the best possible use of theirabilities, the women of the future will have an institu-tionalised childhood and an institutionalised old age, and inbetween a working-life of rush, and nerve-racking strain,trying to fit two full-time professions into a 16-hoursworking dav.

RAHEL LIEBESCHUETZ.

EXPERIMENTAL MYASTHENIA GRAVIS

Sir have followed with interest the work on theattempted production of myasthenia gravis in animals byinjecting them with thymic or muscle extract in Freund’scomplete adjuvant. Dr. Vetters and his colleagues (July 5,p. 28), who were unable to demonstrate the production of anexperimental myasthenia, raise an important point whichDr. Kalden and Dr. Irvine (Sept. 20, p.638) have failed toanswer.

Vetters et al. question the validity of the thymitis, which,as I understand it, is essential for the production of theexperimental disease. The thymitis is diagnosed histologic-ally by observing a dense aggregation of lymphocytesaround Hassall’s corpuscles in the medulla. Goldstein et al.have described these findings in several papers.I-4

I submit that what is described as thymitis is in fact a1. Goldstein, G., Whittingham, S. Lancet, 1966, ii, 315.2. Goldstein, G., Whittingham, S. Clin. exp. Immunol. 1967, 2, 257.3. Oppenheim, T. J., Goldstein, G. Nature, Lond. 1969, 222, 192.4. Goldstein, G., Strauss, A. J. L., Pickeral, S. Clin. exp. Immunol.

1969, 4, 3.

Fig. 1-Normal guineapig thymus with prominent aggregationof lymphocytes around Hassall’s corpuscles in the medulla.

(Hsematoxylin and eosin; x 100.)

Fig. 2-Higher-power view of medulla showing cuff of lympho-cytes around Hassall’s corpuscle.(Haematoxylin and eosin; x 225.)

normal finding, which I have observed on many occasions inthe thymus gland of normal outbred guineapigs (figs. 1 and2). These illustrations are representative of many othernormal thymus glands. They are almost identical to fig. 2bin Goldstein’s recent paper,4 which is said to show thymitis.

I do not feel competent to judge the validity of theelectromyographic data, but I would suggest that whatGoldstein and his associates, and Kalden and Irvine, calla thymitis may be seen in the thymus of normal guineapigs.

It would be unfortunate if a crucial pathological role wasascribed to the thymus in this experimental system, uponthe demonstration of a histological appearance which canbe readily observed in the normal guineapig thymus.

J. N. WEBB.

University Departmentof Pathology,Edinburgh.

TREATMENT OF TETANUS

SIR,-The modern treatment of tetanus outlined byDr. Cole and Dr. Youngman 5 is too expensive to be

adopted in developing countries where the disease is amajor problem. The following is an analysis of the tetanuscases admitted during the 2-year period between Sept.,1967, and Aug., 1969, to the children’s department of thishospital, classified as of grade 2-3 severity by the criteriaof Cole and Youngman.

Apart from general nursing care, antibiotics, and atten-tion to local hygiene and nutrition, the standard manage-ment of these has been with chlorpromazine (2-4 mg. perkg.) given intramuscularly together with paraldehyde (0-2ml. per kg.), and 50,000 units of tetanus antitoxin intra-muscularly 15-20 minutes after the chlorpromazine andparaldehyde. We have encountered no allergic reactionswhen this order has been carefully adopted. 3 further

daily doses of 5000 units of antitoxin were given afteradmission. Spasms were controlled with diazepam(’ Valium ’), 1-2 mg. every 4-6 hours alternating withintramuscular paraldehyde until 48 hours after cessation.

5. Cole, L., Youngman, H. Lancet, 1969, i, 1017.