Jurnal Pityriasis Rosea
Jurnal Pityriasis Rosea
Jurnal Pityriasis Rosea
2
MBChB, CABMS. Al Yarmouk teaching Hospital. [email protected]
3
FICMS, CABMS, DDV. Ibn Sina University for Medical and Pharmaceutical Sciences. [email protected]
Corresponding Email: [email protected]
Abstract
Background: Pityriasis rosea is a common dermatological eruption which is self-limiting with unknown etiology. Many therapeutic
agents have been suggested for its treatment but none of them has gained a uniform consensus. Objective: To assess the efficacy
of erythromycin and prednisolone in reducing the duration of PR. Methods: This is a systematic open placebo-controlled study
and a comparative therapeutic trial conducted through the period from September 2008 to September 2009 in the Department
of Dermatology and Venereology at the Al-Yarmouk Teaching Hospital. Total 75 patients were included in this study and their
demographic information and history of disease, drug and family was recorded. Skin examination was conducted with focus on the
distribution and morphology of the lesions. The patients presented within two weeks of the appearance of their rash were included
and were divided into three groups (25 patients in each group). In group I, adult patients were given erythromycin capsules 250
mg for 4 times per day and children were given erythromycin syrup 25mg/kg in 4 doses/day. Adult patients in group II were
given prednisolone tablets 20mg in two doses daily whereas its 0.5mg a day (2 doses) were given to children. Group III was a
placebo group which received glucose capsules (100mg) four times daily. The duration of treatment was two weeks and every
patient was seen at presentation and asked to attend for evaluation every two weeks until complete disappearance of rash. Results:
In total, 75 patients completed this study of which 44 (58.67%) were females while 31 (41.33%) were males. The mean age of all
patients was 19.19±13.75 years. After two weeks of treatment, the results showed that in erythromycin group, the symptoms got
cleared in 76% of patients at the end of the two weeks as compared to prednisolone group (36%; P=0.005) and placebo group
(12%; P=0.0000064). Prednisolone was found better than placebo with a significant statistical difference (p-value=0.05). The
rash disappeared in 88% & 100% of erythromycin-treated patients, 60% & 84% of prednisolone-treated patients and 24% &
64% in placebo group patients at the end of four and six weeks of therapy respectively. Average number of days for PR to clear
in erythromycin-treated patients was 16.32±8.74 days and in prednisolone-treated patients, it was 26.8±14.69. While in placebo
group, it was 38.8±14.29 (P=0.001). Timing of initiation of treatment, whether it was started within the first week or the second
week, showed minor impact on the course of PR in all therapeutic groups (P=0.26, 0.87 and 0.47 for erythromycin, prednisolone
and placebo group respectively). Conclusions: Both erythromycin and prednisolone are found effective in reducing the duration
of PR; however, erythromycin was found superior to prednisolone.
INTRODUCTION pattern.[1]
The term pityriasis rosea (PR) means pink scales. It is
a common, self-limited, acute dermatological eruption Address for Correspondence: MBChB, CABMS. Al Yarmouk teaching
Hospital. [email protected]
which typically starts as a single oval or rounded scaly Email: [email protected]
plaque on the trunk. Also, smaller daughter lesions along Submitted: 01st August, 2022 Received: 06th August, 2022
the cleavage lines of the trunk appear in Christmas tree Accepted: 23rd August, 2022 Published: 22nd September, 2022
Access this article online This is an open access journal, and articles are distributed under the terms of
the Creative Commons Attribution‑NonCommercial‑ShareAlike 4.0 License,
Quick Response Code:
which allows others to remix, tweak, and build upon the work non‑commercially,
Website:
as long as appropriate credit is given and the new creations are licensed under
www.jnsbm.org
the identical terms.
For reprints contact: [email protected]
DOI: How to cite this article: Salloom A S., Ahmed M J.E., Al-Sudany N K.
10.4103/jnsbm.JNSBM_13_2_3 Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A
Comparative Study. J Nat Sc Biol Med 2022;13:102-109
© 2022 Journal of Natural Science, Biology and Medicine | Published by Wolters Kluwer - Medknow 102
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
Probably, Robert Willan was the first one who described The severity of itching is variable i.e. it is severe in 25%
PR in 1798.[2] of patients, slight to moderate in 50% and absent in 25%.
Minority of PR patients have flu-like illness which is
Epidemiology associated with fever and malaise, headache, joint pain
Pityriasis rosea occurs in all races, and is relatively
and decrease of appetite.[1] Around 69% of the patients
common throughout the world.[1] Its bimodal distribution
show constitutional symptoms[32] while nearly 20% are
is reported in Brazil and Singapore.[3,4] However, some
presented with atypical symptoms.[1] These atypical
studies show no variation in different seasons.[5,6] A study
clinical signs include primary plaque[1], generalized PR[11],
reported its incidence as 0.68 per 100 dermatological
unilateral PR[33], localized PR[34], pityriasis rosea inversa[35],
diseased patients.[7] A community-based study reported
vesicular PR[34], pustular PR[11], urticarial PR[34], purpuric
its incidence as 172.2 per 100.000 person per year.[8]
PR[34], erythema multiforme[36], pityriasis rosea irritate
The disease is more frequent in Africa i.e. about 2% of [7]
and pityriasis rosea gigantia of darier.[7]
all patients examined, however, high variations have
been seen ranging from 2.6% in South Africa to 0.5% in Differential diagnosis of this disease include secondary
Kenya.[9] Although the female: male ratio is 1.5:1,[8] yet, syphilis[1], superficial tinea,[1,34] seborrheic dermatitis[11],
some studies did not find statistically significant variation erythema dyschromicum perstans (Ashy dermatosis)
between both sexes.[10] [34]
, guttate psoriasis[1] and pityriasis lichenoides.[1,11]
Moreover, pityriasis alba[34], viral exanthem[37], tinea
Mostly, the disease is prevalent in patients of age between
versicolor[37], gianoti crosti syndrome[34], erythema
10-35 years, however, it may also occur in infants and in
multiforme[34], urticaria[11], lichen Planus[11] and scabies
the ninth decade of life.[11]
Are also included.(38)
Etiology Treatment
Although the etiology of disease is uncertain, yet so
Erythromycin[38,39] is a bacteriostatic macrolide which is
many clinical and epidemiological features may suggest
used in treating the symptoms of PR. It interferes with
an infective cause.[11] The powerful evidence against the
protein synthesis of bacteria by binding reversibly with
infectious cause is absence of an infectious agent which
50s unit of the ribosome.[40] It shows efficacy against
might be involved in the etiopathogenesis of the disease.[12]
intracellular pathogens by accumulating in macrophages
Some studies also suggest that PR is a viral exanthem that
and leukocytes. It also has immunomodulatory and anti-
is associated with reactivation of HHV-7 and/or HHV-6.[13-
inflammatory efficacy which explains its effect in treatment
15]
Eruptions like PR are also seen in many neoplasms[16-18]
of PR[7] Other than this, acyclovir[41-43] and phototherapy
and bone-marrow transplantation.[19] Moreover, there are
may also benefit patients with PR.[37,44]
drugs which cause PR like eruptions.[11,16,20-29]
Similarly, glucocorticoid which is an oral steroid, is also
Pathogenesis used for treatment of PR.[34] However, some studies have
Examination under electron microscope shows that these reported PR to become worse or even erythrodermic
virions are similar to HHV7. The presence of HHV7 close with its use.[45] Glucocorticoid works by passive diffusion
to the blood vessels in epidermis and dermis depicts that of drug through the cell followed by binding to soluble
the virus may invades the extravascular dermal spaces protein receptor in the cytoplasm.[46] Also, steroid reduces
and cause damage to dermal and epidermal tissues either the synthesis of many pro-inflammatory compounds such
directly or by interaction with the immune system.[30] as ILs, cytokines, proteases and adhesion molecules.
Additionally, DNA of HHV6 and HHV7 is found in [47]
It also effects the division and migration of many
sera of PR patients. Also, their antigens are detected by cells like eosinophils, lymphocytes and monocytes.
using immunohistochemistry and in situ hybridization [48]
Likewise, cell apoptosis may also be triggered by
which confirms the replicative cycle of virus. All those glucocorticoid which can cause lymphocytopenia. [49]s
findings suggest presence of viral infection at least in Glucocorticoid therapy can not only cause leukocytosis
the acute stages of disease.[14,15] HHV7 acts as a primer due to demargination of WBCs from bone marrow[50] but
that provides a transactivating action in the reactivation also inhibition of neutrophil apoptosis.[51] In addition,
of latent HHV 6,[14,31] leading to the impaired detection this therapy also modulates inflammatory processes
of HHV7 in PCR test. This is the reason that HHV6 is such as inhibitory effect on IL1, IL2, IL6 and TNF.[52,53]
detected in skin and many of the body tissues while Additionally, phagocytosis and antigen processing cells
HHV7 is not detected.[31] (macrophages) are inhibited by glucocorticoid[54,55] which
directly affects immediate and delayed hypersensitivity.
Clinical Features
The PR eruption shows a constant course and pattern in Side effects of systemic corticosteroid include pseudotumor
about 80% of cases.[11] In classical presentation, patients cerebri and other psychiatric disorders, skeletal
experience a single truncal patch followed by multiple complications such as myopathy, aseptic bone necrosis,
smaller lesions on the trunk after several days or weeks. fracture and osteoporosis. Cataract with glaucoma is also
Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022 103
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
a complication of cortisol therapy. GIT complications disappearance of the rash. Patients were clearly acquainted
like chronic pancreatitis and perforation and CVS about the disease and its therapy and their consent was
complications like HT, retention of fluid and sodium gained. Also, ethical approval of this study was obtained
andatherosclerosis can also occur. In addition, it can cause from the Ethical Committee of the Scientific Council
dermatological complications like urticaria, anaphylaxis, of Dermatology, Venereology. Iraqi Board for Medical
suppression of hypothalamic-pituitary-adrenal axis, Specialization.
growth failure and secondary amenorrhea.[56]
Statistical Analysis: Statistical analyses were done through
Study aim descriptive and analytic statistics by using Chi-square
To evaluate the effectiveness of erythromycin and and ANOVA considering p-value ≤ 0.05 as significant.[57]
prednisolone in reducing the duration of pityriasis rosea.
Methodology RESULTS
Total 98 patients were recruited in the study, however,
It is a systematic open placebo-controlled and comparative
due to unknown reasons, 75 patients continued with
therapeutic trial study. Total 98 patients were recruited
it. Of these, 44 (58.67%) patients were females and 31
in the study initially, however, 24 of them were dropped
(41.33%) were males and female to male ratio was 1.42:1.
from the study due to unknown reasons and only 75
The mean age of patients was 19.19±13.75 years. Patients
patients continued. The study was conducted in the
in the second decade of their life were the most common
Department of Dermatology, Venereology in Al Yarmouk
age group involved as shown in Figure1 And their age
Teaching Hospital through the period from September
and gender distribution in different therapeutic groups
2008 - September 2009.
is presented in Table 1.
A detailed history of patients was recorded and included
their age, sex, occupation, residence (urban or rural),
season of disease onset, duration at presentation, chief
complaint and other associated symptoms. In addition,
their drug history, previous treatments and personal and/
or family history for such similar conditions was also
obtained. Physical examination was done for every patient
with focus on the type, distribution and number of lesions.
Also all patients were sent to VDRL to exclude syphilis.
Patients were divided into 3 categories (25 individuals in Figure (1): Age and sex distribution of patients with
each): group I patients were given 250mg of erythromycin Pityriasis Rosea.
ethyl succinate (erythromycin, SDI, Samarra, Iraq)
capsules 4 times per daily for adults and 25mg/kg Table 1: Age and sex distribution of PR patients with
erythromycin ethyl succinate syrup (erythromycin, SDI, each therapeutic category.
Samarra, Iraq) four times per day for children for 14 days. Parameter Erythromycin Prednisolone Placebo
Group II patients were given prednisolone (prisolone, SDI, Age
Samarra, Iraq) tablets (10mg) twice daily for adults and Range 4-50 3-51 4-59
Mean 19.08±13.25 18.08±12.60 22.8±15.36
0.5mg/kg twice/day for children for two weeks. Group III
Gender
patients were given glucose capsules 100mg (as placebo)
Male 10(40%) 10(40%) 11(44%)
four times daily for two weeks. Female 15(60%) 15(60%) 14(56%)
104 Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
DISCUSSION
Table 4: PR rash clearance at the end of four weeks. This study was designed to assess two therapeutic agents
Group Cleared/Total % Chi-square (x2) P-value (erythromycin and prednisolone) in cutting short the
20.36 0.0000064* duration of PR. The ages of study participants ranged
Erythromycin 22/25 88
4.99 0.025†
Prednisolone 15/25 60 6.52 0.01**
from 3-59 years with second decade as the most common
Placebo 6/25 24 21.04 0.000027*** age group. This age group is in accordance with a study
*Erythromycin & Placebo which showed that top incidence of this disease occurs in
**Prednisolone & Placebo between 10-35 years old patients.[11] Female:male proportion
†Erythromycin & Prednisolone in current study is 1.42:1 which coincides with other
*** Erythromycin, Prednisolone & Placebo studies,[7,8] whereas there are studies which found equal
Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022 105
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
sex ratio.[10] Another study reported female to male ratio and even cause erythroderma.[56] Whereas in present
in this disease as 1:2.2-3.[58] Clinically, PR was found in study, prednisolone was found effective in PR and no
only 28% of cases under study, whereas in another study, exacerbation of PR was encountered in any of the patients.
the disease was found in 75% of patients.[1] With respect
to the clinical types of PR, the classical variety was the Timing of initiation of treatment, whether it has been
most common (84%) which is somewhat similar to a started within the first week or the second week,
study which reported about 80% of cases as classical.[11] showed minor impact on the course of PR in all study
groups (p-value=0.26, 0.87 and 0.47 for erythromycin,
Despite the cause of PR is not completely known, many prednisolone and placebo group respectively). These
studies have reported the use of antibiotics in the treatment results may be attributed to the limited number of cases
of PR for e.g., erythromycin,[39,58] clarithromycin,[42] recruited in this study. Regarding the side effects, no
azithromycin,[38] and doxycycline.[43] These antibiotics patient encountered any significant unwanted effects
have anti-inflammatory and immunomodulatory effects during the period of treatment, and this goes in parallel
which modify the course of the disease.[7] In present with a study which used erythromycin,[58] however
study, erythromycin was given to patients for two weeks contrasting results were observed with prednisolone in
and it was found that 19 out of 25 (76%) patients were a study.[56]
cleared at the end of two weeks as compared to those
in placebo group P=0.0000064). Similarly, significant
results were obtained at the end of fourth (P=0.0000064)
CONCLUSIONS AND RECOMMENDATIONS
1. Although both oral erythromycin and prednisolone
and sixth week (P=0.0016). The average number of days are effective drugs in shortening the course of PR;
for PR to be cleared in erythromycin treated patients yet, erythromycin is superior to prednisolone.
was 16.32±8.74 days which is highly significant in 2. The use of both oral erythromycin and prednisolone
comparison with prednisolone-treated and placebo-given in recommended doses and duration in this study
patients (P=0.0000001). These findings regarding the showed no significant side effects.
effectiveness of erythromycin in clearing the rash of PR 3. A larger scale study is recommended to assess the
are in accordance with a study in which 73.3% patients effectiveness of erythromycin and prednisolone in
showed complete response with erythromycin[58] higher doses in treatment of PR.
Clarithromycin, a macrolide with a similar action as of
erythromycin, has been reported to fully cure the PR REFERENCES
patients at the end of 28 days.[42] The results of present 1. Blauvelt A. Pityriasis Rosea. In: Wolff K, Goldsmith
study regarding erythromycin coincide with previous LA, Katz SI, Gilchrest BA, Paller AS, Leffell DJ, eds.
studies[42,58] and may indicate its effectiveness in reducing Fitzpatrick’s Dermatology in General Medicine. 7th ed.
the duration of the rash in PR patients. However, there New York, McGraw-Hill Book company; 2008:362-66.
are studies which oppose these findings.[39,48] 2. Weiss L. Pityriasis rosea – an erythematous eruption
of internal origin. Journal of the American Medical
Another antibiotic doxycycline has been investigated in Association. 1903; 41(1): 20-28. doi: https://doi.
an Iraqi placebo-controlled study where 65.2% of the org/10.1001/jama.1903.04470030024006.
patients who were given this antibiotic showed an excellent 3. de Souza Sittart J, Tayah M, Soares Z. Incidence
response i.e. 75% of their rash got disappeared.[43] These pityriasis rosea of Gibert in the Dermatology Service
results coincide with findings of present study taking into of the Hospital do Servidor Publico in the state
account the effectiveness of the antibiotics in PR therapy. of Sao Paulo. Medicina Cutanea Ibero-latino-
americana. 1984; 12(4): 336-38. Available from:
Although virological cause of this disease has been
https://europepmc.org/article/med/6392788.
documented by many studies,[13-15] it is still not confirmed
4. Cheong W, Wong K. An epidemiological study of
yet.[59-61] Similarly, microbial incrimination has also
pityriasis rosea in Middle Road Hospital. Singapore
been disapproved by many studies.[12,62-65] Therefore,
medical journal. 1989; 30(1): 60-62. Available from:
prednisolone is also investigated in this study in treatment
https://europepmc.org/article/med/2595391.
of PR based on that it might be a hypersensitive or
5. Harman M, Aytekin S, Akdeniz S, Serhat İnalöz H. An
reactionary condition. The results revealed it to be better
epidemiological study of pityriasis rosea in the Eastern
than placebo with a significant statistical difference
Anatolia. European journal of epidemiology. 1998; 14(5):
(P=0.05) but less effective than erythromycin (P=0.005).
495-97. doi: https://doi.org/10.1023/A:1007412330146.
The information about the usage of oral corticosteroids 6. Chuh AA, Lee A, Molinari N. Case clustering in
in the treatment of PR is scarce, however, few studies pityriasis rosea: a multicenter epidemiologic study
have recommended the use of systemic corticosteroid for in primary care settings in Hong Kong. Archives of
dermatology. 2003; 139(4): 489-93. Available from:
the widespread, severe and recalcitrant forms of PR.[34,66]
https://jamanetwork.com/journals/jamadermatology/
In contrast, a study reported that it may exacerbate PR
article-abstract/479279.
106 Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
7. Antonio C, Albert L, Vijay Z, Gabriel S, Werner 19. Spelman LJ, Robertson IM, Strutton GM, Weedon
K. Pityriasis rosea-An update. Indian Journal of D. Pityriasis rosea-like eruption after bone marrow
Dermatology, Venereology and Leprology. 2005; transplantation. Journal of the American Academy of
71(5): 311-15. Available from: http://www.bioline. Dermatology. 1994; 31(2, Part 2): 348-51. doi: https://
org.br/abstract?dv05105. doi.org/10.1016/S0190-9622(94)70170-9.
8. Chuang T-YI, Ilstrup DM, Perry H, Kurland LT. 20. Bonnetblanc JM. [Cutaneous reactions to gold salts].
Pityriasis rosea in Rochester, Minnesota, 1969 to Presse Med. Oct 26 1996; 25(32): 1555-8. Réactions
1978: A 10-year epidemiologic study. Journal of the cutanées aux sels d’or. Available from: https://pubmed.
American Academy of Dermatology. 1982; 7(1): 80-89. ncbi.nlm.nih.gov/8952665/.
doi: https://doi.org/10.1016/S0190-9622(82)80013-3. 21. Ghersetich I, Rindi L, Teofoli P, Tsampau D, Palleschi
9. Jacyk WK. Pityriasis rosea in Nigerians. International GM, Lotti T. [Pityriasis rosea-like skin eruptions
Journal of Dermatology. 1980; 19(7): 397-99. doi: caused by captopril]. G Ital Dermatol Venereol.
https://doi.org/10.1111/j.1365-4362.1980.tb03738.x. 1990; 125(10): 457-9. Eruzione cutanea da captopril
10. Björnberg A, Hellgren L. Pityriasis rosea. A “pitiriasi rosea-like”. Available from: https://pubmed.
statistical, clinical, and laboratory investigation ncbi.nlm.nih.gov/2150508/.
of 826 patients and matched healthy controls. Acta 22. Wolf R, Wolf D, Livni E. Pityriasis rosea and
Derm Venereol Suppl (Stockh). 1962; 42(Suppl 50): ketotifen. Dermatology. 1985; 171(5): 355-56. doi:
1-68. doi: https://doi.org/10.2340/0001555542168. https://doi.org/10.1159/000249451.
11. Sterling JC. Viral infections. In: Burns DA, 23. Helfman RJ, Brickman M, Fahey J. Isotretinoin
Breathnach SM, Cox N, Griffiths C, eds. Rook’s dermatitis simulating acute pityriasis rosea. Cutis
Textbook of Dermatology. 7th ed. Oxford: (New York, NY). 1984; 33(3): 297-300. Available
Blackwell Scientific Publications Ltd; 2004:79-83. from: https://pascal-francis.inist.fr/vibad/index.
Available from: https://onlinelibrary.wiley.com/doi/ php?action=getRecordDetail&idt=9594132.
book/10.1002/9780470750520. 24. Corke C, Meyrick T, Huskisson E, Kirby J. Pityriasis
12. Canpolat Kirac B, Adisen E, Bozdayi G, et al. The role of rosea-like rashes complicating drug therapy for rheumatoid
human herpesvirus 6, human herpesvirus 7, Epstein-Barr arthritis. British journal of rheumatology. 1983; 22(3):
virus and cytomegalovirus in the aetiology of pityriasis 187-88. doi: https://doi.org/10.1093/rheumatology/22.3.187.
rosea. J Eur Acad Dermatol Venereol. 2009; 23(1): 16-21. 25. Gupta AK, Lynde CW, Lauzon GJ, Mehlmauer MA,
doi: https://doi.org/10.1111/j.1468-3083.2008.02939.x. Braddock SW, Miller CA. Cutaneous adverse effects
13. DRAGO F, RANIERI E, MALAGUTI E, associated with terbinafine therapy: 10 case reports
BATTIFOGLIO M, LOSI E. Human herpesvirus and a review of the literature. British journal of
7 in patients with pityriasis rosea: Electron dermatology (1951). 1998; 138(3): 529-32. Available
microscopy investigations and polymerase chain from: https://pascal-francis.inist.fr/vibad/index.
reaction in mononuclear cells, plasma and skin. php?action=getRecordDetail&idt=2196642.
Dermatology (Basel). 1997; 195(4): 374-78. Available 26. Buckley C. Pityriasis rosea-like eruption in a
from: https://pascal-francis.inist.fr/vibad/index. patient receiving omeprazole. The British journal
php?action=getRecordDetail&idt=2121623. of dermatology. 1996; 135(4): 660-61. doi: https://
14. Broccolo F, Drago F, Careddu AM, et al. Additional doi.org/10.1111/j.1365-2133.1996.tb03863.x.
evidence that pityriasis rosea is associated with 27. Brazzelli V, Prestinari F, Roveda E, et al. Pityriasis
reactivation of human herpesvirus-6 and-7. Journal rosea–like eruption during treatment with imatinib
of investigative dermatology. 2005; 124(6): 1234-40. mesylate: Description of 3 cases. Journal of
doi: https://doi.org/10.1111/j.0022-202X.2005.23719.x. the American Academy of Dermatology. 2005;
15. Watanabe T, Kawamura T, Aquilino EA, et al. Pityriasis 53(5): S240-S43. doi: https://doi.org/10.1016/j.
rosea is associated with systemic active infection with jaad.2004.10.888.
both human herpesvirus-7 and human herpesvirus-6. 28. Rajpara S, Ormerod A, Gallaway L. Adalimumab‐
Journal of investigative dermatology. 2002; 119(4): 793- induced pityriasis rosea. Journal of the European
97. doi: https://doi.org/10.1046/j.1523-1747.2002.00200.x. Academy of Dermatology and Venereology. 2007;
16. Parsons JM. Pityriasis rosea update: 1986. J Am Acad 21(9): 1294-96. doi: https://doi.org/10.1111/j.1468-
Dermatol. 1986; 15(2 Pt 1): 159-67. doi: https://doi. 3083.2007.02197.x.
org/10.1016/s0190-9622(86)70151-5. 29. Millikan LE. Drug eruptions (dermatitis medicamentosa).
17. Garcia‐F‐Villalta M, Hernández‐Nuñez A, Córdoba S, In: Moschella SL, Hurley HJ, eds. Dermatology. 2nd
Fernández‐Herrera J, García‐Díez A. Atypical pityriasis ed. Philadelphia: WB Saunders Co; 1985.
rosea and Hodgkin’s disease. Journal of the European 30. Drago F, Malaguti F, Ranieri E, Losi E, Rebora
Academy of Dermatology and Venereology. 2004; 18(1): A. Human herpes virus‐like particles in pityriasis
81-82. doi: https://doi.org/10.1111/j.1468-3083.2004.00610.x. rosea lesions: an electron microscopy study. Journal
18. Braveman I. Skin signs of systemic disease. 3rd ed. of cutaneous pathology. 2002; 29(6): 359-61. doi:
Philadelphia: Saunders; 1998. https://doi.org/10.1034/j.1600-0560.2002.290606.x.
Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022 107
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
31. Katsafanas GC, Schirmer EC, Wyatt LS, Frenkel N. 44. Haefeli WE, Schoenenberger RAZ, Weiss P, Ritz
In vitro activation of human herpesviruses 6 and 7 RF. Acyclovir-induced neurotoxicity: Concentration-
from latency. Proceedings of the National Academy side effect relationship in acyclovir overdose. The
of Sciences. 1996; 93(18): 9788-92. doi: https://doi. American Journal of Medicine. 1993; 94(2): 212-15.
org/10.1073/pnas.93.18.9788. doi: https://doi.org/10.1016/0002-9343(93)90186-S.
32. Drago F, Broccolo F, Zaccaria E, et al. Pregnancy 45. Leenutaphong V, Jiamton S. UVB phototherapy for
outcome in patients with pityriasis rosea. Journal of pityriasis rosea: a bilateral comparison study. Journal
the American Academy of Dermatology. 2008; 58(5, of the American Academy of Dermatology. 1995; 33(6):
Supplement 1): S78-S83. doi: https://doi.org/10.1016/j. 996-99. doi: https://doi.org/10.1016/0190-9622(95)90293-7.
jaad.2007.05.030. 46. Esteban NV, Loughlin T, Yergey AL, et al. Daily
33. Del Campo DV, Barsky S, Tisocco L, Gruszka RJ. cortisol production rate in man determined by stable
Pityriasis rosea unilateralis. International journal isotope dilution/mass spectrometry. The Journal of
of dermatology. 1983; 22(5): 312-13. doi: https://doi. Clinical Endocrinology & Metabolism. 1991; 72(1):
org/10.1111/j.1365-4362.1983.tb02146.x. 39-45. doi: https://doi.org/10.1210/jcem-72-1-39.
34. Björnberg A, Tegner E. Pityriasis Rosea. In: Freedberg 47. Werth VP. Systemic Glucocorticoids. In: Goldsmith LA,
IM, Eisen AZ, Wolff K, Austen KF, Goldsmith LA, Katz SI, Gilchrest BA, Paller AS, Leffell DJ, Wolff K, eds.
Katz SI, eds. Fitzpatrick’s Dermatology in General Fitzpatrick’s Dermatology in General Medicine. New
Medicine. New York, NY: The McGraw-Hill York, NY: The McGraw-Hill Companies; 2012:2148-
Companies; 2003:445-50. 53. Available from: https://accessmedicine.mhmedical.
35. Gibney MD, Leonardi CL. Acute papulosquamous com/content.aspx?bookid=392§ionid=41138961.
eruption of the extremities demonstrating an 48. Buttgereit F, Saag K, Cutolo M, da Silva J, Bijlsma J.
isomorphic response. Inverse pityriasis rosea (PR). The molecular basis for the effectiveness, toxicity, and
Arch Dermatol. May 1997; 133(5): 651, 54. doi: https:// resistance to glucocorticoids: focus on the treatment
doi.org/10.1001/archderm.133.5.651. of rheumatoid arthritis. Scandinavian journal of
36. Friedman SJ. Pityriasis rosea with erythema rheumatology. 2005; 34(1): 14-21. doi: https://doi.
multiforme-like lesions. Journal of the American org/10.1080/03009740510017706.
Academy of Dermatology. 1987; 17(1): 135-36. doi: 49. Lu NZ, Cidlowski JA. The origin and functions of
https://doi.org/10.1016/s0190-9622(87)80542-x. multiple human glucocorticoid receptor isoforms. Annals
37. James WD, Berger TG, Elston DM. Andrew’s diseases of the New York Academy of Sciences. 2004; 1024(1):
of the skin E-book: clinical dermatology. 10th ed. 102-23. doi: https://doi.org/10.1196/annals.1321.008.
Canada, WB Saunders Company; 2006. 50. Croxtall JD, Choudhury Q, Flower RJ. Glucocorticoids
38. Amer A, Fischer H. Azithromycin does not cure act within minutes to inhibit recruitment of signalling
pityriasis rosea. Pediatrics. 2006; 117(5): 1702-05. factors to activated EGF receptors through a receptor‐
doi: https://doi.org/10.1542/peds.2005-2450. dependent, transcription‐independent mechanism.
39. Rasi A, Tajziehchi L, Savabi-Nasab S. Oral British journal of pharmacology. 2000; 130(2):
erythromycin is ineffective in the treatment of 289-98. doi: https://doi.org/10.1038/sj.bjp.0703272.
pityriasis rosea. Journal of Drugs in Dermatology: 51. Buttgereit F, Wehling M, Burmester GR. A new hypothesis
JDD. 2008; 7(1): 35-38. Available from: https:// of modular glucocorticoid actions: steroid treatment of
europepmc.org/article/med/18246696. rheumatic diseases revisited. Arthritis & Rheumatism:
40. Christopher C, Gasbarre SK, Schmitt KJ. Tomechi: Official Journal of the American College of Rheumatology.
Antibiotic. In: Wolff K, Goldsmith LA, Katz SI, 1998; 41(5): 761-67. doi: https://doi.org/10.1002/1529-
Gilchrest BA, Paller AS, Leffell DJ, eds. Fitzpatrick’s 0131(199805)41:5%3C761::AID-ART2%3E3.0.CO;2-M.
Dermatology in General Medicine. 7th ed. New York, 52. Groner B, Hynes NE, Rahmsdorf U, Ponta H.
McGraw Hill Book company; 2008:362-6. Transcription initiation of transfected mouse mammary
41. Drago F, Broccolo F, Rebora A. Pityriasis rosea: tumor virus LTR DNA is regulated by glucocorticoid
an update with a critical appraisal of its possible hormones. Nucleic Acids Research. 1983; 11(14):
herpesviral etiology. Journal of the American 4713-25. doi: https://doi.org/10.1093/nar/11.14.4713.
Academy of Dermatology. 2009; 61(2): 303-18. doi: 53. Cupps TR, Fauci AS. Corticosteroid-mediated
https://doi.org/10.1016/j.jaad.2008.07.045. immunoregulation in man. Immunological reviews.
42. Bukhari IA. Oral erythromycin is ineffective in the 1982; 65: 133-55. doi: https://doi.org/10.1111/j.1600-
treatment of pityriasis rosea. J Drugs Dermatol. Jul 065x.1982.tb00431.x.
2008; 7(7): 625. Available from: https://pubmed.ncbi. 54. Cidlowski JA, King KL, Evans-Storms RB, Montague
nlm.nih.gov/18664152/. JW, Bortner CD, Hughes Jr FM. The biochemistry and
43. Ghassaq AT. Doxycycline in the treatment of pityriasis molecular biology of glucocorticoid-induced apoptosis
rosea. Thesis for fellowship of Iraqi Commission in the immune system. Recent Progress in Hormone
for Medical Specialization in Dermatology and Research. 1996; 51: 457-90; discussion 90. Available
Venereology; 2000. from: https://europepmc.org/article/med/8701091.
108 Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022
Treatment of Pityriasis Rosea With Erythromycin and Prednisolone: A Comparative Study
Journal of Natural Science, Biology and Medicine ¦ Volume 13 ¦ Issue 2 ¦ January-December 2022 109