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Kumar, Anagha Bangalore

0000-0002-3615-6432

Mayo Clinic

Department of Dermatology, Mayo Clinic, Rochester, Minnesota, USA.

Citations 7

Mohs Micrographic Surgery for Invasive Melanoma Allows for Tissue Preservation Compared With Wide Local Excision: A Retrospective Cohort Study
Rames, Melissa M. , Campbell, Elliott H. , Asamoah, Eucabeth, Trischman, Thomas , Kumar, Anagha , Vidal, Nahid Y. , Demer, Addison M. , Kumar, Anagha Bangalore , Demer, Addison

Dermatologic Surgery | June 18, 2024 | Volume: 50 | Issue: 11 | Pages: 997-999

10.1097/dss.0000000000004270 Get It

BACKGROUND While increasing evidence supports the safety and effectiveness of immunohistochemistry-assisted Mohs micrographic surgery (MMS) for superficially invasive melanoma, there is a paucity of the literature investigating its effect on final defect size. OBJECTIVE To evaluate the tissue sparing effect of MMS for melanoma. MATERIALS AND METHODS Three hundred and twenty-eight patients with early-stage (T1a/T1b) cutaneous melanomas treated with MMS from January 2008 to December 2018 were evaluated. Measured defect sizes after Mohs tumor extirpation were compared with anticipated defect size that would result from standard-margin wide local excision (WLE). Average actual versus anticipated defect areas were compared using a paired t-test (95% confidence intervals). RESULTS The following groups demonstrated a significantly smaller defect area for MMS-treated tumors when compared with anticipated standard-margin WLE defect: All tumors combined (13.8 cm2 vs 10.4 cm2, p < .001), tumors requiring 1 stage (13.6 cm2 vs 10.1 cm2, p < .001), and tumors requiring 2 stages (13.2 cm2 vs 10.5 cm2, p = .004). The majority of patients (83.5%, n = 274) achieved clear margins with 1 stage. CONCLUSION Immunohistochemistry-assisted MMS for early-stage invasive melanoma is associated with smaller final defect size and overall tissue sparing effect compared with standard WLE margins.
Reply to “BASCULE syndrome: Additional evidence for the association with autonomic dysfunction”
Reinhart, Jacob P. , Kumar, Anagha , Rooke, Thom W. , Sartori‐Valinotti, Julio C. , Tollefson, Megha M. , Klaas, Kelsey , Davis, Dawn Marie R. , Kumar, Anagha Bangalore , Sartori-Valinotti, Julio C., Davis, Dawn M R , Reinhart, Jacob , Casanegra, Ana I.

Pediatric Dermatology | May 14, 2024 | Volume: 41 | Issue: 3 | Pages: 566-566

10.1111/pde.15549 Get It

Bridging the gap in BASCULE syndrome: A retrospective case series of a recently described clinical entity
Reinhart, Jacob P. , Kumar, Anagha , Casanegra, Ana I. , Rooke, Thom W. , Sartori‐Valinotti, Julio C. , Tollefson, Megha M. , Klaas, Kelsey , Davis, Dawn Marie R. , Kumar, Anagha Bangalore , Davis, Dawn M R , Casanegra, Ana I , Reinhart, Jacob

Pediatric Dermatology | November 28, 2023 | Volume: 41 | Issue: 1 | Pages: 46-50

10.1111/pde.15470 Get It

AbstractBackgroundBier anemic spots, cyanosis with urticaria‐like eruption (BASCULE) syndrome is a recently described entity with episodic urticarial lesions and white anemic halos on a background of erythrocyanosis, commonly affecting the lower extremities. Possible association with autonomic dysfunction remains poorly understood. Existing publications are limited, but the condition is suggested as highly underrecognized.ObjectiveTo further characterize clinical and epidemiologic data for BASCULE syndrome.MethodsWe performed an IRB‐approved retrospective chart review on patients with BASCULE syndrome evaluated at Mayo Clinic from April 2021 to November 2022.ResultsA total of 17 patients were identified (13 female, 4 male). Median age of onset was 12 years (range 9–17). Lower extremities were involved in all patients (17). Most patients were symptomatic with pruritus (8) or burning pain (8); three were asymptomatic. Triggers were standing (11), hot showers or hot environments (7), or no clear trigger (4). Autonomic dysfunction was present in 10 patients. Treatment responses were observed from propranolol (3) and high‐dose cetirizine (1).ConclusionNovel epidemiologic data from 17 pediatric and young adult patients with BASCULE syndrome further supports an association with autonomic dysfunction and suggests a higher prevalence than previously acknowledged.
Results of Patch Testing to Botanicals: Review of the Mayo Clinic Experience over 2 Decades (1997–2017)
Kumar, Anagha , Jin, Mauricio F. , Kunkel, Hilary, Sathe, Nishad, Hall, Matthew R. , Drage, Lisa A., Youssef, Molly J. , Yang, Yul W. , Yiannias, James A. , Killian, Jill M. , Davis, Mark D.P. , Youssef, Molly, Killian, Jill, Kumar, Anagha Bangalore

Dermatitis® | November 27, 2023 | Volume: 35 | Issue: 1 | Pages: 43-48

10.1089/derm.2023.0109 Get It

Abstract: Background: Botanicals are increasingly incorporated into skincare products. Although allergic contact dermatitis due to botanicals is recognized, data describing the prevalence of positive patch tests to botanicals are sparse. Objective: To report the Mayo Clinic experience of patch testing to selected botanical products in the standard, extended standard, fragrance, and plant series. Methods: IRB-approved retrospective study of the Mayo Clinic experience with patch testing to botanicals from 1997 to 2017. Results: In total, 12,169 people were patch tested to botanicals in the standard, extended standard, fragrance, and plant series; 4032 were men and 8137 were women. The mean age of the population tested was 54 (standard deviation 17.7) years. Almost 11% (1320/12,169) of the patch-tested population exhibited positive reactions to at least 1 botanical agent. Myroxylon pereirae resin 25% was the most common positive allergen in the series. Patients who had positive reactions to at least 1 botanical agent were more (19.8%) likely to have a positive reaction to at least 1 additional botanical than those patients who did not have any positive tests. Most patients presented with generalized involvement (334) or involvement of the hands (284) or face (232). Conclusion: Physicians should be aware of the high prevalence of allergic contact dermatitis and patch test positivity associated with botanical products.
Reactive granulomatous dermatitis as a clinically relevant and unifying term: a retrospective review of clinical features, associated systemic diseases, histopathology and treatment for a series of 65 patients at Mayo Clinic
Kumar, Anagha , Lehman, Julia S. , Johnson, Emma F. , Cantwell, Hafsa M. , Sartori‐Valinotti, Julio C. , Davis, Mike , Wetter, David A. , Kumar, Anagha Bangalore , Johnson, E F , Wetter, D A , Lehman, Julia S , Sokumbi, Olayemi , Davis, M.D.P.

Journal of the European Academy of Dermatology and Venereology | May 10, 2022 | Volume: 36 | Issue: 12 | Pages: 2443-2450

10.1111/jdv.18203 Get It

Abstract Background Reactive granulomatous dermatitis (RGD) is an umbrella term used to describe interstitial granulomatous dermatitis (IGD), palisaded neutrophilic and granulomatous dermatitis (PNGD), and interstitial granulomatous drug eruption (IGDR). Objective The aim of this study was to describe systemic associations of RGD, explore possible associations between histopathologic findings and systemic RGD associations and determine clinical relevance of RGD subtypes. Methods We retrospectively studied clinical and histopathologic characteristics of patients with RGD from 1990 through 2020. Results Of 65 patients with RGD (41 women, 24 men; median age at diagnosis, 62 years), 37 had IGD, 26 had PNGD, and 2 had IGDR. Fifty patients (76.9%) had an associated systemic condition; rheumatologic conditions were identified for 34 (52.3%) patients. The associated systemic condition occurred before RGD in approximately 75% of patients. Statistical analyses did not show significant associations between specific subtypes of RGD and systemic diseases or treatment response, and specific histopathologic findings were not predictive of an associated systemic disease. Conclusions Although most patients with RGD had an associated systemic condition, subtypes of RGD did not correlate with systemic associations, lending support to the use of the umbrella term RGD .
Rethinking the prescription of biotin for dermatologic conditions
Kumar, Anagha , França, Katlein , França, Katlein , Kumar, Anagha Bangalore , Lotti, Torello

Dermatologic Therapy | May 22, 2018 | Volume: 31 | Issue: 4 | Pages: e12618

10.1111/dth.12618 Get It