|Year : 2019 | Volume
| Issue : 1 | Page : 6
First report of a disease by rhazes 10 centuries ago
Rouzbeh R Ghafouri1, Mostafa Araj-khodaei2, Somaiyeh T Targhi2, Mojtaba Varshochi3, Zahra Parsian1, Reza Yarani4, Samad E J. Golzari5
1 Emergency Medicine Research Team, Tabriz University of Medical Science, Tabriz, Iran
2 Aging Research Institute, Tabriz University of Medical Science, Tabriz, Iran
3 Department of Infectious Diseases, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
4 Department of Pediatrics E, Copenhagen Diabetes Research Center (CPH-DIRECT), Herlev University Hospital, Herlev, Denmark
5 Department of Anesthesiology and Intensive Care Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
|Date of Submission||11-May-2017|
|Date of Acceptance||18-Jun-2018|
|Date of Web Publication||15-Jan-2019|
Department of Emergency Medicine, Tabriz University of Medical Sciences, Daneshgah Street, Tabriz - 51664
Source of Support: None, Conflict of Interest: None
Introduction: Abu Bakr Mohammad Ibn Zakariya Al-Razi (865–925 CE), who was known as “Rhazes” in the west, was a famous scientist of medieval ages. He has more than 200 books and treatises. His masterpiece on medicine “Kitab Al-Hawi Fi Al-Tibb” contains around 900 case reports. Some of the diseases which seem to be recently reported have been stated previously, but not well described. Considering symptoms of the patient described at that time, differential diagnosis will be discussed. Case presentation: Rhazes described a patient with bilious fever. He had developed bloody urine and stool on the fourth day and fatigue. Subsequently, the patient's urine and stool color turned into dark and black, respectively, and died the following day. According to Rhazes attitude, it was malignant measles. Meyerhof in his book has referred to post-measles acute glomerulonephritis, but more appropriate differential diagnoses are compatible with this patient. Discussion: One of the best diagnoses for this case can be Weil's syndrome. Presence of fever, icterus, hemorrhage and renal injury, all suggest Weil's syndrome without pulmonary involvement. The other probable diagnosis is thrombotic thrombocytopenic purpura (TTP). Meningococcal sepsis is the other possible diagnosis. Conclusion: To sum up, as three compatible diseases with the case; have been described more than a thousand years after Rhazes (Weil's syndrome 1886, TTP 1925 and meningococcemia 1805); if the case is either Weil's or TTP or meningococcal sepsis, it is the first report of the disease in the world by Rhazes.
Keywords: Malignant measles, meningococcemia, post-measles acute glomerulonephritis, Rhazes, thrombotic thrombocytopenic purpura, Weil's disease
|How to cite this article:|
Ghafouri RR, Araj-khodaei M, Targhi ST, Varshochi M, Parsian Z, Yarani R, J. Golzari SE. First report of a disease by rhazes 10 centuries ago. Int J Prev Med 2019;10:6
|How to cite this URL:|
Ghafouri RR, Araj-khodaei M, Targhi ST, Varshochi M, Parsian Z, Yarani R, J. Golzari SE. First report of a disease by rhazes 10 centuries ago. Int J Prev Med [serial online] 2019 [cited 2019 Dec 16];10:6. Available from: http://www.ijpvmjournal.net/text.asp?2019/10/1/6/250288
| Introduction|| |
Persian medicine is one of the doctrines of medicine and its origin pretends to about 10,000 years ago. Persian medicine physicians not only assembled previous data but also added their own experiences to them.,
Abu Bakr Mohammad Ibn Zakariya Al-Razi (865–925 CE), known in west as “Rhazes,” was one of those Persian polymathes well-known for his immense contributions to the different fields of the science including but not limited to the chemistry, medicine, philosophy, astronomy, music and mathematics.,
He has written more than 200 books and treatises about variety of topics. His masterpiece, “Kitab Al-Hawi Fi Al-Tibb” (a comprehensive textbook of medical practice and treatment) commonly known as Liber continents in Europe, has been taught for centuries as a basic educational source at medical schools. It is an encyclopedia on practical medicine that was gathered by Rhazes and includes his precedent scholars' opinions such as Hippocrates and Galen. In this book, approximately 900 case reports have been presented as an educational aid for the documentation of different diseases.
Thirty-three of these case presentations have been gathered in the book: “Al-Ghesas- val-Hekayat-al-Marza” (tales and stories of patients) by Meyerhof. Some of the diseases which seem to be recently reported have been stated previously, but not well described.
The case which is presented in this article died from an acute illness; seemingly, an interesting case and perhaps the first to report this disease. Accordingly, the original excerpt from the original book is presented, followed by the signs and symptoms of the disease and probable diagnoses.
“A patient named Bani bin Sawada had a bilious fever. Bilious fever is a fever that ensues from bilious hummer excess. After 4 days, his urine became bloody and his stool changed to bloody green bile similar to blood of fresh meat; the patient suffered from fatigue. The patient's condition was steady until the night, but deteriorated and the disease recurred with the same severity. I suspected that he drank something. That day evening his urine and stool became black. On the sixth day, he died. He had malignant measles which had spread into his internal organs.”
Rhazes described a patient with bilious fever (the patient had fever and icterus). He had developed bloody urine (i.e., hematuria) and stool (i.e., hematochezia) on the fourth day. He defined the appearance of the stool as fresh meat blood. The patient complained of fatigue which indicates generalized weakness.
According to what Rhazes has described, this disease was uncommon and unknown at the time and no new remarkable symptoms were observed until the fourth day. Subsequently, the patient's condition deteriorated and his urine and stool color turned into dark and black, respectively. Reference to dark urine might pertain to a subsequent acute glomerulonephritis or acute tubular necrosis or probably gross hematuria. Also, black stool (melena) might have been a manifestation of gastrointestinal (GI) bleeding which ultimately changed to hematochezia on fifth day. The patient died in the morning of the sixth day.
From Rhazes' point of view, it was malignant measles which spread to the victim's internal organs. Since he has referred to measles, the patient must have had rashes which have not been mentioned directly in the case. To summarize, the patient had fever, icterus, fatigue, melena, hematuria and rashes with rapid progression to death.
Meyerhof remarked this collection of symptoms to be related to post-measles acute glomerulonephritis; nevertheless, considering the symptoms and presence of rectal bleeding, more appropriate differential diagnoses might be compatible with this patient. Fever, back pain, anxiety, insomnia, cough, headache and skin lesions are manifestations of measles according to ancient medicine.
| Discussion|| |
There are some diagnoses for the reported case that can explain the patient's symptoms and acuteness of the disease which culminated in death. One of the best diagnoses for this case can be severe form of leptospirosis, Weil's syndrome. This syndrome is an infectious disease caused by leptospira. It is presented with a wide scope of symptoms and is a worldwide, sporadic and zoonosis disease. It has abrupt onset with an incubation period of 2–20 days. Five-to-ten percent of patients show multi-organ failure, while others experience mild and subclinical form of the disease. At all ages, symptoms include fever, myalgia and headache. Other presentations are lethargy, emesis, abdominal pain, photophobia, arthralgia, cough, diarrhea or constipation.
Lung involvement can be seen in fatal Weil's syndrome, which is not mentioned in the case. Some articles have mentioned pulmonary involvement as the cause of death in 55% and other studies have shown that mortality rate reaches to 74% when lungs are affected. Severe pulmonary hemorrhage syndrome is the major cause of death in Weil's syndrome in developing countries. Others are acute renal failure and also widespread hemorrhage.
Another study that has been performed on 150 patients with Weil's syndrome concluded the following results: renal involvement in 100%, hemorrhagic syndrome in 50%, neurologic presentation in 48%, atypical pneumonia in 44% and GI involvement in 21%.
Presence of fever, icterus, hemorrhage and acute renal injury in the patient, all suggest the conclusion that the patient had Weil's syndrome without pulmonary involvement. Although pulmonary involvement is a common cause of death in this syndrome, it can accrue without affecting lungs as well. Since Rhazes did not report any other similar cases, it seems as if the disease was of sporadic nature which is compatible with leptospirosis.
The other probable diagnosis is thrombotic thrombocytopenic purpura (TTP). TTP is a multi-system disease which is diagnosed on the base of progressive appearance of the following symptoms: microangiopathic hemolytic anemia, thrombocytopenia, fever, neurologic and renal problems.
Prior to the effective treatment with plasma exchange, 90% of patients died from systemic microvascular thrombosis that caused cerebral and myocardial infarction and renal failure. Although GI bleeding and icterus are not encompassed in pentad of TTP, they can be found in the course of the disease. Rhazes patient, in addition to fever and renal involvement, suffered hemorrhage and icterus which can ensue from thrombocytopenia and hemolysis, respectively. Therefore, TTP could also be suggested for the patient. If Rhazes statement on measles is interpreted as purpura, it strengthens the diagnosis of TTP.
Meningococcal sepsis is the other possible diagnosis of the patient. Meningococcal sepsis can cause hypotension, disseminated intravascular coagulation, multiple-organ failure and osteonecrosis. Rash – which is petechial, purpuric or maculopapular and arthritis are other signs of meningococcal disease.[21–23] The disease is fatal without appropriate treatment. The patient's signs and symptoms can all be seen in meningococcemia and icterus can be a result of end organ failure in the progression of the disease.
Another disease with hemorrhagic fever is dengue fever with mortality rate of 50% if untreated. It is transmitted through mosquito bite and causes bleeding from mucus membranes, which is not prominent in this case; and the patient had icterus which is not a manifestation in dengue fever, all of which question the diagnosis of dengue fever. The classical presentation of dengue fever is arthralgia, fever, headache and rash but our patient did not have either headache or arthralgia.
| Conclusion|| |
To sum up, three diseases are compatible with the case: Weil's syndrome, TTP and meningococcemia. The first one has been described in 1886 by Weil in Germany, TTP in 1925 and meningococcemia in 1805.
Since the reported case had a progressive course and high mortality rate and terminated in death in 6 days without receiving any treatment, according to the symptoms of patient, these diagnoses seem more probable. More accurate diagnoses could have been suggested if Rhazes had described more details about the patient such as: age, occupation, past medical history, appearance of probable skin lesion and presence of pulmonary and neurologic symptoms. If the case is either Weil's or TTP or meningococcal sepsis, it is the first report of the disease in the world by Rhazes.
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| References|| |
Khodaei MA, Ghaffari F, Emadi F, Emaratkar E, Alijaniha F, Noorbala AA, et al
. Healthy lifestyle in Prevention and Treatment of Depression from the View of Iranian Traditional Medicine. Med Hist J 2017;9:169-92.
Khodaei MA, Noorbala AA, Parsian Z, Targhi ST, Emadi F, Alijaniha F, et al
. Avicenna (980-1032CE): The pioneer in treatment of depression. Transylvanian Rev 2017; 17: 4377-89.
Golzari SE, Khan ZH, Ghabili K, Hosseinzadeh H, Soleimanpour H, Azarfarin R, et al
. Contributions of medieval Islamic physicians to the history of tracheostomy. Anesth Analg 2013;116:1123-32.
Nezhad GS, Dalfardi B. Rhazes (865–925AD), the icon of Persian cardiology. Int J Cardiol 2014;177:744-7.
Zargaran A, Azizi A, Kordafshari G, Borhani-Haghighi A. Rhazes Contribution to the Role of Nutrition in Preventive Medicine and Public Health. Iranian J Public Health 2014;43:1461-2.
Ashtiyani SC, Shamsi M, Cyrus A, Tabatabayei SM. Rhazes, a Genius Physician in the Diagnosis and Treatment of Nocturnal Enuresis in Medical History. Iranian Red Crescent Med J 2013;15:633.
Zarshenas MM, Mehdizadeh A, Zargaran A, Mohagheghzadeh A. Rhazes (865–925 AD). J Neurol 2012;259:1001-2.
Meyerhof M. Thirty-three clinical observations by Rhazes (circa 900 AD). Isis 1935;23:321-72.
Hall KS, Kusunoki Y, Gatny H, Barber J. Social Discrimination, Stress, and Risk of Unintended Pregnancy Among Young Women. J Adolesc Health 2015;56:330-7.
Bruce MG, Sanders EJ, Leake JA, Zaidel O, Bragg SL, Aye T, et al
. Leptospirosis among patients presenting with dengue-like illness in Puerto Rico. Acta Tropica 2005;96:36-46.
Tilahun Z, Reta D, Simenew K. Global epidemiological overview of leptospirosis. Int J Microbiol Res 2013;4:9-15.
Katz AR, Ansdell VE, Effler PV, Middleton CR, Sasaki DM. Assessment of the clinical presentation and treatment of 353 cases of laboratory-confirmed leptospirosis in Hawaii, 1974–1998. Clin Infect Dis 2001;33:1834-41.
Organization WH. Human leptospirosis: Guidance for diagnosis, surveillance and control. 2003.
da Rocha Medeiros F, Spichler A, Athanazio DA. Leptospirosis-associated disturbances of blood vessels, lungs and hemostasis. Acta Tropica 2010;115:155-62.
Chakrabarti A, Nandy M, Pal D, Mallik S. A rare case of Weil's disease with alveolar haemorrhage. Asian Pac J Trop Biomed 2014;4:S66-9.
Fabri M. Clinical manifestations of leptospirosis. Int J Infect Dis 2010;14:e164.
Garcia MM, de Diego Damia A, Villanueva RM, Hontagas JL. Pulmonary involvement in leptospirosis. Eur J Clin Microbiol Infect Dis 2000;19:471-4.
George JN. Thrombotic thrombocytopenic purpura. N Engl J Med 2006;354:1927-35.
Blehar DJ, Dickman E, Gaspari R. Identification of congestive heart failure via respiratory variation of inferior vena cava diameter. Am J Emerg Med 2009;27:71-5.
Campbell WN, Joshi M, Sileo D. Osteonecrosis following meningococcemia and disseminated intravascular coagulation in an adult: Case report and review. Clin Infect Dis 1997;24:452-5.
Stephens DS, Hajjeh RA, Baughman WS, Harvey RC, Wenger JD, Farley MM. Sporadic meningococcal disease in adults: Results of a 5-year population-based study. Ann Intern Med 1995;123:937-40.
Parmentier L, Garzoni C, Antille C, Kaiser L, Ninet B, Borradori L. Value of a novel Neisseria meningitidis–specific polymerase chain reaction assay in skin biopsy specimens as a diagnostic tool in chronic meningococcemia. Arch Dermatol 2008;144:770-3.
Schaad UB. Arthritis in disease due to Neisseria meningitidis. Rev Infect Dis 1980;2:880-8.
Brandtzaeg P, van Deuren M Classification and pathogenesis of meningococcal infections. Neisseria meningitidis: Advanced Methods and Protocols. 2012:21-35.
Gubler DJ. Dengue and dengue hemorrhagic fever. Clin Microbiol Rev 1998;11:480-96.
Dalugama C, Shelton J, Ekanayake M, Gawarammana IB. Dengue fever complicated with Guillain-Barré syndrome: A case report and review of the literature. J Med Case Rep 2018;12:137.