Dermatology: Practical and Conceptual Research | Dermatol Pract Concept 2016;6(3):5 17 DERMATOLOGY PRACTICAL & CONCEPTUAL www.derm101.com Introduction Dermoscopy is gaining popularity in the diagnosis of inflam- matory dermatoses. Polarized dermoscopes are widely used due to their better visualization of the deeper epidermis and papillary dermis [1]. A granulomatous disorder is a pathological description of a variety of conditions that have different etiologies but Dermoscopy could be useful in differentiating sarcoidosis from necrobiotic granulomas even after treatment with systemic steroids Shahira Ramadan1, Dalia Hossam1, Marwah A. Saleh1 1 Dermatology Department Cairo University, Cairo, Egypt Key words: cutaneous sarcoidosis, dermoscopy, necrobiotic granuloma, steroids, treatment Citation: Ramadan S, Hossam D, Saleh MA. Dermoscopy could be useful in differentiating sarcoidosis from necrobiotic granulomas even after treatment with systemic steroids. Dermatol Pract Concept 2016;6(3):5. doi: 10.5826/dpc.0603a05 Received: August 2, 2015; Accepted: May 24, 2016; Published: July 31, 2016 Copyright: ©2016 Ramadan et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Funding: None. Competing interests: The authors have no conflicts of interest to disclose. All authors have contributed significantly to this publication. Corresponding author: Marwah Adly Saleh, MD, PhD, Department of Dermatology, Cairo University School of Medicine, Kasr Al Ainy Hospital, PO 11956, Cairo, Egypt. Tel. +201223132773. Email: salehmarwah@kasralainy.edu.eg Background: Diagnosing cutaneous sarcoidosis and necrobiotic granulomas is challenging. Objective: Assessing the value of dermoscopy in differentiating cutaneous sarcoidosis from necro- biotic granulomas and evaluating whether their dermoscopic features will be altered after treatment. Methods: Nineteen cutaneous sarcoidosis and 11 necrobiotic granuloma patients (2 necrobiosis li- poidica, 4 granuloma annulare and 5 rheumatoid nodule) were included in this study. The diagnosis was confirmed by skin biopsy. The lesions were examined using non-contact polarized dermoscope (Dermlite 2 HR-Pro; 3Gen, San Juan Capistrano, CA). Results: Ten out of 19 cutaneous sarcoidosis patients and 7/11 necrobiotic cases group were receiving treatments (topical, intralesional or systemic steroids ± chloroquine) but still have cutaneous lesions. Treatment duration in the sarcoidosis group ranged from 2 months to 10 years (median 3 years) and in the necrobiotic cases group ranged from 3 months to 16 years (median 2 years). Pink homogenous background, translucent orange areas, white scar-like depigmentation and fine white scales were sig- nificantly associated with the cutaneous sarcoidosis compared to necrobiotic cases group. On the other hand mixed pink, white and yellowish background was significantly associated with the necro- biotic cases group. No significant difference in the dermoscopic findings was detected between treated and non-treated patients. Conclusion: Some dermoscopic findings are shared between the cutaneous sarcoidosis group and the necrobiotic cases group, yet dermoscopy could be a useful aid in differentiating them even after treatment. ABSTRACT mailto:salehmarwah@kasralainy.edu.eg 18 Research | Dermatol Pract Concept 2016;6(3):5 was represented using the terms sensitivity, specificity, +ve predictive value, -ve predictive value, and overall accuracy. P values less than 0.05 was considered statistically significant. All statistical calculations were done using computer program SPSS (Statistical Package for the Social Science; SPSS Inc., Chicago, IL, USA) release 15 for Microsoft Windows (2006). 2.2 Accuracy calculations Sensitivity = T(+)ve ÷ [T(+)ve + F(-)ve] Specificity = T(-)ve ÷ [T(-)ve + F(+)ve] Positive predictive value = T(+)ve ÷ [T(+)ve + F(+)ve] Negative predictive value = T(-)ve ÷ [T(-)ve + F(-)ve] Overall accuracy = [T(+)ve + T(-)ve] ÷ All sample Results The demographic data of the patients are summarized in Table 1. Nineteen cutaneous sarcoidosis cases and 11 nec- robiotic cases groups (2 necrobiosis lipoidica, 4 granuloma annulare and 5 rheumatoid nodule) were included in this study. The number of examined lesions in the cutaneous sar- coidosis group ranged from 1 to 16 lesions (median=3). The number of examined lesions in the necrobiotic cases group (necrobiosis lipoidica, granuloma annulare and rheumatoid nodule) ranged from 1 to 14 lesions (median=2). Ten out of 19 cutaneous sarcoidosis cases and 7/11 of the necrobiotic cases group were receiving treatments but still had cutaneous lesions. The cutaneous sarcoidosis patients received systemic steroids and chloroquine. One patient received adjuvant intralesional steroids. Three patients from the necrobiotic cases group received topical steroids, 1 patient received systemic steroids, 2 patients received systemic ste- roids and methotrexate and 1 patient received systemic steroids, methotrexate and chloroquine. The dermoscopic findings are summarized in Table 2. The results showed that pink homogenous background, translucent orange areas, white scar-like depigmentation and fine white scales (Figure 1) were significantly associated with cutaneous sarcoidosis compared to the necrobiotic share granuloma formation pathologically. A granuloma is an organized collection of epithelioid histiocytes with vari- able number of multinucleated giant cells [2]. Granulomas include sarcoidal, foreign body granuloma and necrobiotic granuloma [3]. Necrobiotic granulomas include granuloma annulare, necrobiosis lipoidica, rheumatoid nodules, rheuma- toid fever nodules and foreign body reactions. The diagnosis of cutaneous sarcoidosis is challenging due to the variety of clinical presentations of the disease [4]. Moreover, differentiating cutaneous sarcoidosis from necro- biotic granulomas is sometimes difficult [5], and the existence of both conditions in the same patient was already reported [6]. In this work we aimed to assess the value of dermoscopy in differentiating cutaneous sarcoidosis from necrobiotic granulomas. Patients and methods This is a cross sectional study that was conducted between January and November 2014 in our department. All patients diagnosed as cutaneous sarcoidosis or necrobiotic granulo- mas during this period were included in this study. Patients were subjected to history taking, clinical examination, and skin biopsy to confirm the diagnosis and dermoscopic exami- nation using polarized dermoscope (Dermlite 2 HR-Pro). This study was approved by the ethical committee of the Dermatology Department and was conducted according to the declaration of Helsinki principles. 2.1 Statistical analysis Data were statistically described in terms of mean ± standard deviation (± SD), median and range, or frequencies (number of cases) and percentages when appropriate. Comparison of numerical variables between the study groups was done using Mann-Whitney U test for independent samples. For compar- ing categorical data, Chi square (χ2) test was performed. Exact test was used instead when the expected frequency was less than 5. Correlation between various variables was done using Spearman’s rank correlation equation. Accuracy TABLE 1. Demographic data of the patients [Copyright: ©2016 Ramadan et al.]   Cutan Cutaneous sarcoidosis (n=19) eous sarcoidosis (n=19) Necrobiotic cases group (n=11) Females 16 8 Males 3 3 Age (mean) 25-62 (45±9.8) 18-69 (37.7±17.1) Fitzpatrick’s skin type (number) IV (18), V (1) IV (7), V (2), VI (2) Disease duration range (median) 2 months-10 years (3 years) 3 months- 16 years (2 years) Total number of examined lesions (range, median) 1-16 (3) 1-14 (2) Research | Dermatol Pract Concept 2016;6(3):5 19 TABLE 2. Summary of the dermoscopic findings [Copyright: ©2016 Ramadan et al.] Cutaneous sarcoidosis (n=19) Necrobiotic cases group P value Granuloma annulare (n=4) Necrobiosis lipoidica (n=2) Rheumatoid nodule (n=5) Background color Pink homogenous background 14 0 0 3 *0.018 Mixed pink and white homogenous background 0 1 0 1 0.298 Mixed pink, white and yellowish background 0 2 2 0 *0.012 Mixed pink and orange background 5 0 0 0 0.082 Translucent orange globules and areas Translucent orange globules 4 0 0 0 0.141 Translucent orange areas 12 0 0 0 *0.001 Blood vessels Arborizing vessels 5 0 2 1 0.637 Short linear blood vessels 9 0 2 1 0.245 Pigmentation Hypopigmented areas 0 2 0 0 0.367 Scar like depigmentation 7 0 0 0 *0.025 Reticulate pigmentation 1 1 2 1 *0.047 Scales Fine white scales 9 0 0 0 *0.006 *P value <0.05 is significant Figure 1. Dermoscopic picture of cutaneous sarcoidosis cases showing (a) arborizing blood vessels (black arrow) (no treatment); (b) translucent orange areas (black arrow) (treatment for 3 years); (c) scar-like depigmentation (black arrow) (no treatment); (d) white scales (black arrow) (no treatment). [Copyright: ©2016 Ramadan et al.] 20 Research | Dermatol Pract Concept 2016;6(3):5 Discussion The spectrum of inflammatory diseases that can be diagnosed using a dermoscope has markedly increased. Granulomatous skin diseases are a group of inflammatory dermatoses that are characterized pathologically by granuloma formation. Few studies evaluated the use of dermoscopy in diagnosing cuta- neous sarcoidosis; the largest of which was using 7 cases [7]. In this work we aimed to assess the value of the dermoscope in diagnosing cutaneous sarcoidosis using a larger number of patients. Moreover, we tried to evaluate whether receiving cases group. P values were 0.018, 0.001, 0.025 and 0.006 respectively. On the other hand, mixed pink, white and yellowish background was significantly associated with the necrobiotic cases group; p value was 0.012 (Figure 2). We tried to evaluate whether receiving treatment affected the dermoscopic findings. We compared the dermoscopic findings of the patients who were receiving treatment with those who had not started any treatment. However, the results were not significant in all the dermoscopic findings (Table 3) (Figure 3). Figure 2. Dermoscopic picture of necrobiotic cases group (a) necrobiotic granuloma showing mixed pink, white and yellowish background and arborizing blood vessels (black arrow) (no treatment); (b) granuloma annulare showing hypopigmented areas (black arrow) (no treatment); (c) rheumatoid nodule showing mixed pink and white background and short linear vessels (black arrow) (treatment for 2 years). [Copyright: ©2016 Ramadan et al.] TABLE 3. Comparison between dermoscopic findings in treated and untreated cases [Copyright: ©2016 Ramadan et al.]   Cutaneous sarcoidosis (n=19) Necrobiotic cases group (n=11)   Untreated cases (9) Treated cases (10) P value Untreated cases (4) Treated cases (7) P value Background color Pink homogenous background 5 9 0.119 0 3 0.212 Mixed pink and white homogenous background 0 0 0 2 0.382 Mixed pink, white and yellowish background 0 0 3 1 0.088 Mixed pink and orange background 4 1 0.119 0 0 Translucent orange globules and areas Translucent orange globules 1 3 0.333 0 0 Translucent orange areas 7 5 0.22 0 0 Blood vessels Arborizing vessels 4 1 0.119 1 2 0.721 Short linear blood vessels 4 5 0.586 1 2 0.721 Pigmentation Hypopigmented areas 0 0 2 0 1 Scar like depigmentation 2 5 0.22 0 0 Reticulate pigmentation 0 1 0.526 2 2 0.47 Scales Fine white scales 5 4 0.414 0 0 Research | Dermatol Pract Concept 2016;6(3):5 21 authors stated that arborizing blood vessels were detected in necrobiosis lipoidica while linear vessels were detected in sarcoidosis. Nonetheless, we detected arborizing blood vessels in 5 (26.3%) cases of cutaneous sarcoidosis. Those arboriz- ing blood vessels might be shorter with fewer branches in sarcoidosis than necrobiosis lipoidica. Necrobiosis lipoidica is a rare disease. Bakos et al. [12], Pellicano et al. [11] and Lallas et al. [13] all reported the presence of arborizing vessels on yellowish background in necrobiosis lipoidica, and our results confirm their findings. Hairpin like structures were detected by Bakos et al. in necro- biosis lipoidica; although we did not detect any hair pin like structures, we noticed that short linear blood vessels can be seen in necrobiosis lipoidica patients. Lallas et al [13]reported the dermoscopic findings of granuloma annulare in 47 lesions of 24 patients. They found that the dermoscopic findings in granuloma annulare are heterogeneous. The background color is a combination of red and white in 42.6%, dotted vessels in 40.4%, short linear vessels in 21% and arborizing vessels in 14.9% of the lesions. In this work we found mixed pink and white background in 1 patient. Interestingly we found hypopigmented areas in 2/4 granuloma annulare patients and mixed pink white and yellow background in 1 patient. Some dermoscopic features of inflammatory lesions are lost after treatment with steroids, which makes their diagnosis difficult [14]. Regarding lichen planus, Wickham’s striae and peripheral homogenous vascular pattern disappeared after 4 weeks of treatment with topical steroids [14]. Interestingly, our results showed that the dermoscopic findings of cutane- ous sarcoidosis and necrobiotic cases group remained even after several years of treatment. Some possible explanations are that topical and systemic steroids may not be effective in treating all patients [15] or that more time may be needed for these lesions to disappear. In addition to that, different drugs with different mechanisms of action may be responsible for different dermoscopic modifications after treatment. treatment affected the dermoscopic findings of cutaneous sarcoidosis and necrobiotic granulomas. Pellicano et al. [7] reported that scar-like depigmentation and translucent orange globules were suggestive of cutane- ous sarcoidosis. They detected scar-like depigmentation in 5 cases and translucent orange globules in 7 cases of cutaneous sarcoidosis. The translucent orange globules were thought to be equivalent to the apple jelly color in diascopy [8]. Our results showed that scar-like depigmentation was detected in 7/19 (36.8%) cutaneous sarcoidosis cases, which was statisti- cally significant in differentiating cutaneous sarcoidosis from necrobiotic granuloma; p value was 0.025. In our results, trans- lucent orange globules were found in 4/19 (21.1%) cutaneous sarcoidosis cases. Although they were not detected in any nec- robiotic granuloma, they were not significant in differentiating cutaneous sarcoidosis from the necrobiotic cases group. On the other hand, our results added that translucent orange areas were significant in differentiating cutaneous sar- coidosis from the necrobiotic cases group; p value was 0.001. Translucent orange areas were 100% specific and 63.16% sensitive in differentiating cutaneous sarcoidosis from nec- robiotic granulomas. However, in spite of their significance, they might not be specific for sarcoidosis. Translucent orange areas were reported before in lupus vulgaris [9]. Interestingly, differentiating sarcoidosis from lupus vulgaris clinically and pathologically is challenging. Therefore it is not surprising that they have the similar dermoscopic features. Vazquez-Lopez et al. [10] reported the presence of vas- cular globules in 2 cutaneous sarcoidosis cases. Vascular globules were not detected in this work. Moreover, Pellicano et al. and Vazquez-Lopez et al. reported that linear vessels were associated with sarcoidosis. In this work we detected short linear vessels in 9 (47%) cutaneous sarcoidosis cases and in 3 (27%) of the necrobiotic group. However, the results were not significant. Arborizing blood vessels were the main clue to differentiate necrobiosis lipoidica from sarcoidosis according to Pellicano et al. [11] and Lallas et al. [8]. Those Figure 3. Treatment did not affect the dermoscopic findings of cutaneous sarcoidosis. Translucent or- ange areas in the forehead of a non-treated male (a) and a treated female for 3 years with systemic steroids (b). [Copyright: ©2016 Ramadan et al.] 22 Research | Dermatol Pract Concept 2016;6(3):5 systemic sarcoidosis. Ann Dermatol 2012;24:74-6. PMID: 22363160. DOI: 10.5021/ad.2012.24.1.74. 6. Igawa K, Maruyama R, Satoh T, et al. Necrobiosis lipoidica-like skin lesions in systemic sarcoidosis. J Dermatol 1998;25:653-6. PMID: 9830264. DOI: 10.1111/j.1346-8138.1998.tb02475.x. 7. Pellicano R, Tiodorovic-Zivkovic D, Gourhant JY, et al. Der- moscopy of cutaneous sarcoidosis. Dermatology 2010;221:51-4. PMID: 20375489; DOI: 10.1159/000284584. 8. Lallas A, Giacomel J, Argenziano G, et al. Dermoscopy in gen- eral dermatology: practical tips for the clinician. Br J Dermatol 2014;170:514-26. PMID: 24266695. DOI: 10.1111/bjd.12685. 9. Brasiello M, Zalaudek I, Ferrara G, et al. Lupus vulgaris: a new look at an old symptom—the lupoma observed with dermos- copy. Dermatology 2009;218:172-4. PMID: 19060460. DOI: 10.1159/000182255. 10. Vazquez-Lopez F, Palacios-Garcia L, Gomez-Diez S, Argenziano G. Dermoscopy for discriminating between lichenoid sarcoid- osis and lichen planus. Arch Dermatol 2011;147:1130. PMID: 21931067. DOI: 10.1001/archdermatol.2011.278. 11. Pellicano R, Caldarola G, Filabozzi P, Zalaudek I. Dermoscopy of necrobiosis lipoidica and granuloma annulare. Dermatology 2013;226:319-23. PMID: 23797090. DOI: 10.1159/000350573. 12. Bakos RM, Cartell A, Bakos L. Dermatoscopy of early-onset nec- robiosis lipoidica. J Am Acad Dermatol. 2012;66:e143-4. PMID: 22421129. DOI: 10.1016/j.jaad.2011.01.028. 13. Lallas A, Zaballos P, Zalaudek I, et al. Dermoscopic patterns of granuloma annulare and necrobiosis lipoidica. Clin Exp Dermatol 2013;38:425-7. PMID: 23495727 DOI: 10.1111/ced.12126. 14. Gungor S, Topal IO, Goncu EK. Dermoscopic patterns in active and regressive lichen planus and lichen planus variants: a morpho- logical study. Dermatol Pract Concept. 2015;5(2): 45-53. PMID: 26114051. DOI: 10.5826/dpc.0502a06. 15. Katoh N, Mihara H, Yasuno H. Cutaneous sarcoidosis successful- ly treated with topical tacrolimus. Br J Dermatol. 2002;147:154- 6. PMID: 12100200. 10.1046/j.1365-2133.2002.04727.x. Some limitations of this work should be highlighted: dermoscopic features before and after treatment have not been compared; the limited number of patients, especially in the necrobiotic cases group; and most of the patients were Fitzpatrick’s skin type IV skin phototype. In conclusion, some dermoscopic findings are shared between the cutaneous sarcoidosis and necrobiotic cases group. However, translucent orange areas, white scar-like depigmentation and white scales may be more suggestive of cutaneous sarcoidosis, while mixed pink, white and yellowish background may be more suggestive of necrobiotic granu- loma. The dermoscopic features of cutaneous sarcoidosis might remain even after receiving treatment. Acknowledgment The authors acknowledge Dr. Magdy Ibrahim, Professor of Obstetrics and Gynecology at Cairo University for his help with statistics. References 1. Marghoob AA, Usatine RP, Jaimes N. Dermoscopy for the family physician. Am Fam Physician 2013;88:441-50. PMID: 24134084. 2. Weedon D, Strutton G, Rubin AI, Weedon D (eds). Weedon’s Skin Pathology. 3rd ed. London: Churchill Livingstone, 2010. 3. Hawryluk EB, Izikson L, English JC, 3rd. Non-infectious granu- lomatous diseases of the skin and their associated systemic dis- eases: an evidence-based update to important clinical questions. Am J Clin Dermatol 2010;11:171-81. PMID: 20184390. DOI: 10.2165/11530080-000000000-00000. 4. Katta R. Cutaneous sarcoidosis: a dermatologic masquerader. Am Fam Physician 2002;65:1581-4. PMID: 11989634. 5. Chiba T, Takahara M, Nakahara T, et al. Cutaneous sarcoid- osis clinically mimicking necrobiosis lipoidica in a patient with