Home | Register | Login | Inquiries | Alerts | Sitemap |  

Advanced Search
JKM > Volume 34(2); 2013 > Article
Kwon, Jang, Cho, Lee, Kim, and Woo: Successful Treatment of Two Patients with Immune Thrombocytopenic Purpura Using Herbal Decoction



This case report was conducted to introduce the effectiveness of herbal decoction on patients with chronic immune thrombocytopenic purpura (ITP).


We closely observed two patients who were admitted to the Department of Internal Medicine 1 of Kyung-Hee Korean Medical Hospital due to ITP. We gave a herbal decoction to these patients and then analyzed the changes in their general conditions as well as blood test results.

Results and Conclusions:

The treatment with herbal decoctions was helpful for ITP patients.


Immune thrombocytopenic purpura is an acquired disorder. The two criteria required for its diagnosis are normal complete blood count and white blood cell differential, including a normal peripheral blood smear, and no clinically apparent associated conditions that may cause thrombocytopenia1).
The pathogenesis of ITP is thought to be related to increased platelet destruction with inhibition of platelet production through the production of specific autoantibodies. However, such antibodies are not demonstrable in all patients, and assays for antiplatelet antibodies have not been important for management decisions2).
The incidence of ITP is highest in children, and may be greater in boys than in girls3). In adults, the incidence increases with age. The incidence in women is greater than in men at the age under 60, but in adults age over 60, the incidence in men is the same as in women4).
When deciding to treat an ITP patient, a threshold platelet count of 30,000/microL for clinical decisions, rather than a range of platelet counts, is presented. However, clinical symptoms and patients’ concerns are more important for treatment decisions. Usually, glucocorticoids are the first line therapy, but IVIG (intra-venous immuno-globulin) may also be used as the first line instead of glucocorticoids when a more rapid increase in platelet count is required. After taking glucocorticoids, many patients may suffer from adverse effects such as weight gain, fluid retention insomnia, Cushingoid facies, dorsal fat, diabetes, osteoporosis, and so on5).
In addition to these ordinary therapies, herbal medicine can be effective in treating these patients. Now we report one child and one adult ITP patient who have shown improvement while taking herbal decoction.

Case Presentation

  1. Case 1

    • (1) Name: Huh ○ ○, M/7

    • (2) O/S: 2010. 7.

    • (3) C/C: ① rhinorrhea from allergy rhinitis ② fatigue

    • (4) P/H: N

    • (5) F/H: N

    • (6) P/I: In July 2010, the patient’s platelet count was 30,000 when examined at Ewha Womans University Hospital. There, he was diagnosed with ITP and started to take glucocorticoid. He was injected with IVIG 3 times. The last treatment was done in July 2011. He also had visited a local Korean medicine clinic to take a herbal decoction, which was not effective.

    • (7) Treatment

    • Jiyuseongyangtang (JYSYT-地楡升陽湯)1 - 1ch#3, 50cc (Table 1)

    • ② Acupuncture: N

    • (9) Lapse

    • ① Duration of treatment: 2011. 09. 30 ∼ 2013.02.26

    • ② Laboratory data

  2. Case 2

    • (1) Name: Nam Kung ○, M/21

    • (2) O/S: 2010. 9

    • (3) C/C: ① purpura ② petechiae

    • (4) P/H: Admission to local hospital for about 1 month due to a car accident when 10 years old.

    • (5) F/H: Father HTN

    • (6) P/I: In September 2010, he found several purpura lesions on his skin and visited a local dermatologic clinic. The doctor advised him to get a thorough medical examination at another, bigger hospital. He went to Seoul St. Mary’s hospital and was diagnosed with ITP. At that time, his platelet was 5,000 10^3/μL and he started to take glucocorticoid.

    • (7) Treatment

    • Jiyuseongyangtang (JYSYT地楡升陽湯)2 - 2ch#3, 100cc (Table 2)

    • ② Acupuncture: N

    • (9) Lapse

    • ① Duration of Treatment: 2011.05.31 ∼ 2013.03.04

    • ② Laboratory data

Treatment results

There is no gold standard test that can confirm ITP. The diagnosis is a consequence of exclusions, which requires that other causes of thrombocytopenia be ruled out. A presumptive diagnosis of ITP is made when the history, physical examination, complete blood count, and examination of the peripheral blood smear do not suggest other causes for the patient’s isolated thrombocytopenia1.
Two patients were diagnosed as ITP at other university hospitals. When they came to Kyunghee Korean medicine hospital, both of them submitted medical certificates diagnosed with ITP. Since ITP appears only with abnormal platelet counts, we regularly checked only CBC counts of each patient while we gave herbal decoctions.
The 5-year-old child patient was 123cm tall and weighed 25kg when he first came to our clinic. He had normal appetite, bowel and urine habits. However, he frequently complained about rhinorrhea from allergy rhinitis, fatigue, and bad feelings at every seasonal changing time. His face was pale, and pulse was weak, thin, and quite tight. He had been tapering off prednisolone to 2.5 mg qd. We prescribed him JYSYT1 (table 1) from September 23, 2011. We divided 1 chup (帖) into 3 packs (包) for this 5 year-old boy, adjusting the concentration of the decoction to be milder than for an adult patient. His platelet count started to rise once he started taking this medicine. This rising tendency continued for about 3 months, despite him quitting prednisolone on February 3, 2012. However, after suffering from a severe cold in September 2012, his platelet count dropped again to around 80,000 for a couple of months. When we examined his platelet count on January 7, 2013, it was 180,000, which was already over the normal limit.
The adult patient was 178cm tall and weighed 69kg. He had normal appetite and urine habits. He had sporadic constipation, and often suffered from dyspepsia. Once he decided to take herbal medicine, he quit taking prednisolone and concentrated on our therapy. We prescribed him JYSYT2 (Table 2) from February 15, 2011. We divided 2 chup (帖) into 3 packs (包). Though his platelet count had fluctuated during treatment, the overall tendency had been gradually rising, and the final platelet count was 162,000 at February 23, 2013.


The pathogenesis of ITP is related to a combination of increased platelet destruction along with inhibition of megakaryocyte platelet production via the production of specific IgG autoantibodies by the patient’s B cells, most often directed against platelet membrane glycoproteins such as GPIIb/IIIa2,6,7).
ITP is a common acquired bleeding disorder. The incidence of ITP in children is greater than the incidence among adults8).
Understanding of the natural history of untreated ITP, which differs between children and adults, provides part of the rationale to decide which patients should be treated. Many children receive no specific therapy, since 70 to 80 percent have a spontaneous complete remission of the disease within six months.
Approximately 70 percent of children have the acute form of ITP, which is defined by recovery of presentation within six months with or without treatment. Pharmacologic intervention, when used, is directed toward the early control of symptoms, such as stopping severe hemorrhage or minimizing the risk of significant bleeding. Such therapy does not affect the long-term outcome9,10).
ITP in adults is typically a chronic disease, the prevalence exceeds the incidence. In one estimate of the prevalence of ITP in the US, the estimate was approximately 100 per million per year, with age cohorts ranging from 41 to 160 per million per year, with the highest values seen in the oldest cohort11).
Spontaneous remissions are unusual in adults, occurring in 9 percent in one series. The necessity for treatment in adults varies with the severity of the thrombocytopenia12).
The incidence of major bleeding and death from bleeding is also unknown, although these events are thought to be rare. The absence of firm data on these important clinical outcomes hinders all management decisions12,13,14).
Since major bleeding is rare and primarily occurs in those with platelet counts below 10,000/microL15), the goal for treatment of ITP is to provide a safe platelet count to prevent major bleeding, rather than returning the platelet count to normal16,17,18).
However, the rationale for continued therapy is uncertain among asymptomatic patients with chronic severe thrombocytopenia who have had no or only a partial response to one or more treatment regimens. Unnecessary treatment of asymptomatic patients with mild to moderate thrombocytopenia, platelet count greater than 30,000/microL, should be avoided, because ITP may be a more benign disease than previously thought, and may be best approached by a conservative treatment program in the majority of patients19).
Treatment to increase the platelet count is always initiated in patients with a platelet count below 30,000/microL, which is severe enough to constitute a risk of bleeding. Glucocorticoids are the preferred agents for first-line therapy, while splenectomy, rituximab, and thrombopoiesis-stimulating agent s are typically reserved for second or third-line therapy20,21,22).
When approaching children ITP, the ASH guidelines (published in 1996) suggest that no therapeutic intervention is generally needed for children with platelet counts greater than 30,000/microL as they are unlikely to have serious bleeding. Pharmacologic therapy is recommended for any child with significant bleeding regardless of the platelet count and with platelet counts less than 10,000/microL and cutaneous bleeding23).
Unlike in western medicine, there is no specific term or definition which refers to ITP in Korean medicine. However, in Donguibogam (東醫寶鑑) there are some records describing purpura or petechia24). It also says that these features seem to be related to weak spleen (脾虛), shrunken yin (陰虛), and heated blood (血熱). These states are all associated with blood flow. From this point of view, they already have understood this phenomenon as the malfunction of blood cells or a disorder of the blood stream25).
Therefore, the goal of treating ITP is not only preventing bleeding and bruising but also recovering normal platelet count, taking care of each patient’s individual conditions.
Both patients’ prescriptions were based on JYSYT. The fundamental decoction of JYSYT is Ikweeseongyangtang (IWSYT, 益胃升揚湯). We added Sookjihwang (熟地黃) to raise yin (陰) and blood (血), and increased Jiyu (地楡) to prevent bleeding signs. IWSYT consists of Bojungikgitang (BJIGT, 補中益氣湯) and Hwanggeum (黃芩), and BJIGT is a famous prescription for those who are lacking in ki (氣虛). We thought the major cause of ITP for these two people was weak spleen (脾虛).
We used JYSYT1 to the child patient. His ki (氣) was so insufficient that he was sensitive to seasonal changes, complained about fatigue, and frequently caught cold. His pulse was weak and thin. This is why we put more Baekchul (白朮) and added Insam (人參).
We gave JYSYT2 to the adult patient. We put in more Sookjiwhang (熟地黃) than the child patient, because we thought he had shrunken yin (陰.) He sweated while sleeping, his cheek turned pink when he was tired or talking, and felt intermittent thirst. We also put in a small amount of Siho (柴胡) to bring down this mild heat (陰虛熱).
There are other reports which describe the effectiveness of herbal decoctions in ITP patients허 All the cases showed improvements whether parallel therapy with glucocorticoid was done or not27,28,29). However, the starting point of rising platelet count seems to be shorter in those who did not use glucocorticoid.
Since there is only a small chance to encounter ITP patients in local Korean medicine clinics, we must demonstrate the effectiveness of herbal medicine from just a few case reports. This report is also made to let people know the high possibility of herbal decoction in treating ITP patients. From this point of view, lack of number of patients is a limitation to generalizing to all kinds of ITP patients. Therefore, we should continue to study this disease through experiments in vivo or in vitro. We should investigate the specific steps, clarifying how platelet disorders recover to normal stage. After that, a clinical research should be prepared to prove these experiments. Since we have seen that herbal decoction can be a good remedy to ITP patients, regardless of age and sex, we hope that further study can be carried out soon.

Fig. 1
Change of platelet count (10^3/μL) of the child patient
Fig. 2
Change of platelet count (10^3/μL) of the child patient
Table 1
Jiyuseongyangtang(JYSYT-升麻)1-1ch#3, 50cc
Herb Scientific name Dose (g)
Jiyu (地楡) Sanguisorbae Radix 12
Baekchul (白朮) Atractylodis Rhizoma Alba 12
Cheukbaekyup (側柏葉(炭)) Thujae Orientalis Folium 12
Danggui (當歸) Angelica acutiloba Kitagawa 6
Sookjiwhang (熟地黃) Rehmanniae Radix Preparata 6
Sansa (山査) Crataegi Fructus 6
Jinpi (陳皮) Citri Unshii Pericarpium 6
Insam (人參) Ginseng Radix Alba 3
Chunma (天麻) Gastrodiae Rhizoma 3
Sain (沙仁) Amomi Fructus 3
Gamcho (甘草) Glycyrrhizae Radix 3
Whanggeum (黃芩) Scutellariae Radix 2
Seungma (升麻) Cimicifugae Rhizoma 2
Table 2
Jiyuseongyangtang(JYSYT-陰)2-2ch#3, 100cc
Herb Scientific name Dose (g)
Sookjiwhang (熟地黃) Rehmanniae Radix 12
Jiyu (地楡) Sanguisorbae Radix 8
Cheukbaekyup (側柏葉(炭)) Thujae Orientalis Folium 8
Baekchul (白朮) Preparata Atractylodis Rhizoma Alba 6
Danggui (當歸) Angelica acutiloba Kitagawa 6
Sansa (山査) Crataegi Fructus 4
Jinpi (陳皮) Citri Unshii Pericarpium 4
Maeka (麥芽) Hordei Fructus Germinatus 4
Sain (沙仁) Amomi Fructus 4
Gamcho (甘草) Glycyrrhizae Radix 3
Seungma (升麻) Cimicifugae Rhizoma 2
Siho (柴胡) Bupleuri Radix 2
Hwanggeum (黃芩) Scutellariae Radix 1


1. British Committee for Standards in Haematology General Haematology Task Force. Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy. Br J Haematol. 2003; 120:574
crossref pmid

2. Cines DB, Blanchette VS. Immune thrombocytopenic purpura. N Engl J Med. 2002; 346:99

3. Frederiksen H, Schmidt K. The incidence of idiopathic thrombocytopenic purpura in adults increases with age. Blood. 1999; 94:909

4. Zeller B, Rajantie J, Hedlund-Treutiger I, Tedgård U, Wesenberg F, Jonsson OG, et al. Childhood idiopathic thrombocytopenic purpura in the Nordic countries: epidemiology and predictors of chronic disease. Acta Paediatrica. 2005; 94:178
crossref pmid

5. Provan D, Stasi R, Newland AC, Blanchette VS, Bolton-Maggs P, Bussel JB, et al. International consensus report on the investigation and management of primary immune thrombocytopenia. Blood. 2010; 115:168
crossref pmid

6. Michel M, Lee K, Piette JC, Fromont P, Schaeffer A, Bierling P, et al. Platelet autoantibodies and lupus-associated thrombocytopenia. Br J Haematol. 2002; 119:354
crossref pmid

7. Kuwana M, Kaburaki J, Okazaki Y, Miyazaki H, Ikeda Y. Two types of autoantibody-mediated thrombocytopenia in patients with systemic lupus erythematosus. Rheumatology (Oxford). 2006; 45:851
crossref pmid

8. Zeller B, Rajantie J, Hedlund-Treutiger I, Tedgård U, Wesenberg F, Jonsson OG, et al. Childhood idiopathic thrombocytopenic purpura in the Nordic countries: epidemiology and predictors of chronic disease. Acta Paediatr. 2005; 94:178
crossref pmid

9. Kühne T, Buchanan GR, Zimmerman S, Michaels LA, Kohan R, Berchtold W, et al. A prospective comparative study of 2540 infants and children with newly diagnosed idiopathic thrombocytopenic purpura (ITP) from the Intercontinental Childhood ITP Study Group. J Pediatr. 2003; 143:605
crossref pmid

10. Rosthøj S, Hedlund-Treutiger I, Rajantie J, Zeller B, Jonsson OG, Elinder G, et al. Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: A prospective Nordic study of an unselected cohort. J Pediatr. 2003; 143:302
crossref pmid

11. Segal JB, Powe NR. Prevalence of immune thrombocytopenia: analyses of administrative data. J Thromb Haemost. 2006; 4:2377
crossref pmid

12. Stasi R, Stipa E, Masi M, Cecconi M, Scimò MT, Oliva F, et al. Long-term observation of 208 adults with chronic idiopathic thrombocytopenic purpura. Am J Med. 1995; 98:436
crossref pmid

13. Portielje JE, Westendorp RG, Kluin-Nelemans HC, Brand A. Morbidity and mortality in adults with idiopathic thrombocytopenic purpura. Blood. 2001; 97:2549
crossref pmid

14. Neylon AJ, Saunders PW, Howard MR, Proctor SJ, Taylor PR. Clinically significant newly presenting autoimmune thrombocytopenic purpura in adults: a prospective study of a population-based cohort of 245 patients. Br J Haematol. 2003; 122:966
crossref pmid

15. Lacey JV, Penner JA. Management of idiopathic thrombocytopenic purpura in the adult. Semin Thromb Hemost. 1977; 3:160

16. George JN, Woolf SH, Raskob GE, Wasser JS, Aledort LM, Ballem PJ, et al. Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology. Blood. 1996; 88:3

17. Rodeghiero F, Stasi R, Gernsheimer T, Michel M, Provan D, Arnold DM, et al. Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group. Blood. 2009; 113:2386
crossref pmid

18. Toltl LJ, Arnold DM. Pathophysiology and management of chronic immune thrombocytopenia: focusing on what matters. Br J Haematol. 2011; 152:52
crossref pmid

19. Guidry JA, George JN, Vesely SK, Kennison SM, Terrell DR. Corticosteroid side-effects and risk for bleeding in immune thrombocytopenic purpura: patient and hematologist perspectives. Eur J Haematol. 2009; 83:175

20. British Committee for Standards in Haematology General Haematology Task Force. Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy. Br J Haematol. 2003; 120:574
crossref pmid

21. Provan D, Stasi R, Newland AC, Blanchette VS, Bolton-Maggs P, Bussel JB, et al. International consensus report on the investigation and management of primary immune thrombocytopenia. Blood. 2010; 115:168
crossref pmid

22. Neunert C, Lim W, Crowther M, Cohen A, Solberg L, Crowther MA. The American Society of Hematology 2011 evidence-based practice guideline for immune thrombocytopenia. Blood. 2011; 117:4190
crossref pmid

23. George JN, Woolf SH, Raskob GE, Wasser JS, Aledort LM, Ballem PJ, et al. Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology. Blood. 1996; 88:3

24. Hujun . Donguibogam. Seoul: Bubinmunhwasa;2007. p. 799

25. Korean Medicine College Hepatology faculty. Hepato-internal medicine. Seoul: Dongyang medical Publishing Company;2013. p. 616p. 620–21.

27. Choi MY, Lee SB, Kim SH, Kim YC, Lee JH, Woo HJ. A case report of ITP in a child patient. The Society of Korean Oriental Internal Medicine. 2007; 200–206.

28. Han CW, Kim CW, Lee JE, Rhy KR, Kim YC, Lee JH, et al. Therapeutic response of herbal medicine in 8 adult patients with idiopathic thrombocytopenic purpura. The Society of Korean Oriental Internal Medicine. 2004; 82–94.

29. Park SM, Seong HS, Han CW, Kim DW, Kim YC, Lee JH, et al. A clinical report on 5 cases of ITP in adults administered herbal medicine. The Korean Society for Oriental Internal Medicine. 2002; 187–192.

Editorial office contact information
3F, #26-27 Gayang-dong, Gangseo-gu Seoul, 157-200 Seoul, Korea
The Society of Korean Medicine
Tel : +82-2-2658-3627   Fax : +82-2-2658-3631   E-mail : skom1953@daum.net
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Developed in M2PI