Year :
2023
| Month :
May
| Volume :
17
| Issue :
5
| Page :
WD03 - WD05
Full Version
Acral Acanthosis Nigricans with Concurrent Vitamin B12 Deficiency in an Indian Patient: An Atypical Presentation
Published: May 1, 2023 | DOI: https://doi.org/10.7860/JCDR/2023/61029.17878
Pihu Sethi, Kriti Maheshwari, Shalini Bahadur, Shivani Kalhan
1. Assistant Professor, Department of Dermatology, Venereology and Leprosy, Government Institute of Medical Sciences, Greater Noida, Uttar Pradesh, India.
2. Senior Resident, Department of Dermatology, Venereology and Leprosy, Government Institute of Medical Sciences, Greater Noida, Uttar Pradesh, India.
3. Professor, Department of Pathology, Government Institute of Medical Sciences, Greater Noida, Uttar Pradesh, India.
4. Professor and Head, Department of Pathology, Government Institute of Medical Sciences, Greater Noida, Uttar Pradesh, India.
Correspondence Address :
Dr. Kriti Maheshwari,
Senior Resident, Department of Dermatology, Venereology and Leprosy, Government Institute of Medical Sciences, Greater Noida, Uttar Pradesh, India.
E-mail: maheshwari.kriti@gmail.com
Abstract
Acanthosis Nigricans (AN) is characterised by velvety, papillomatous, brownish-black, hyperkeratotic plaques, typically on the intertriginous areas and neck. It is more commonly seen in people of African American descent and rarely occurs in the Indian population. The present case includes a 28-year-old male who presented to the Outpatient Department with asymptomatic hyperpigmentation over the skin of both feet and knuckles of both hands for three months. The distribution pattern over the knuckles was suggestive of vitamin B12 deficiency; however, the atypical distribution over the feet leads to suspicion of a differential diagnosis of lichen planopigmentosus, vitamin B12 deficiency, and acral AN. Dermoscopy was done to aid in the diagnosis and revealed linear crista cutis and sulcus cutis, which are features suggestive of AN. On investigation, serum vitamin B12 levels were below 100 μg/mL, and histologic sections showed hyperkeratosis with papillomatosis and mild acanthosis. The patient was treated solely with 1500 mcg mecobalamine daily for ten days and followed-up. The dermoscopic and histopathological findings were consistent with the diagnosis of acral AN, and thus a final diagnosis of acral AN superimposed with vitamin B12 deficiency was made. This case is being reported due to its rare occurrence in the Indian population, the atypical clinical presentation of AN in the form of macules, and to highlight dermoscopy as an essential non-invasive tool aiding in the diagnosis. The diagnosis of acral AN should not be overlooked despite the finding of low serum vitamin B12 levels in such a case, and the authors wish to create awareness among clinicians to investigate the patient further.
Keywords
Dermoscopy, Hyperpigmentation, Pigmentary disorders
Case Report
A 28-year-old male, apparently healthy and moderately built, presented to the Outpatient Department with asymptomatic hyperpigmentation over the skin of bilateral feet and bilateral knuckles for three months. The pigmentation started over the medial side of the left foot initially and then progressed to involve other sites. The patient had no history of occupational exposure to coal tar, chemicals or dyes, no previous medications prior to the onset of lesions, or any significant family history. On examination, multiple ill-defined hyperpigmented macules, some coalescing to form large macules, were present on the dorsum of the feet, metatarsophalangeal joints, and metacarpophalangeal joints in a bilaterally symmetrical manner (Table/Fig 1). The 3rd, 4th, and 5th fingernails of the right hand and the fourth fingernail of the left hand showed subungual hyperkeratosis and onycholysis. Mucocutaneous examination of other sites revealed no abnormalities. General physical examination was normal, and the patient’s Body Mass Index (BMI) was 22.03 kg/m2. There were no systemic features suggestive of diabetes or other endocrinopathies.
Dermoscopy was done due to the atypical distribution of the lesions considering a differential diagnosis of lichen planopigmentosus, B12 deficiency and acral AN. Dermoscopic examination revealed linear crista cutis and sulcus cutis which was suggestive of AN (Table/Fig 2). KOH examination was positive confirming the diagnosis of onychomycosis (Table/Fig 3). Complete blood count with peripheral smear, fasting and postprandial blood sugar, thyroid profile and routine urine analysis were within normal limits. Serum insulin level was within normal limits. Ultrasonography of whole abdomen revealed no abnormalities. Serum B12 levels were below 100 μg/mL.
Skin biopsy was performed and haematoxylin and eosin stained histologic sections showed orthokeratotic hyperkeratosis, acanthosis along with papillomatosis. The valley between the papillae is filled with keratotic material [Table/Fig-4,5]. Patient was treated solely with 1500 mcg mecobalamine daily for 10 days and followed-up. No other oral or topical medication was prescribed at this stage. The hyperpigmented macules on metacarpophalangeal joint and metatarsophalangeal joints showed significant improvement in the pigmentation over a short duration of 10 days (Table/Fig 6). The dermoscopic and histopathological findings were consistent with the diagnosis of AN and thus a final diagnosis of acral AN superimposed with vitamin B12 deficiency was made.
Discussion
AN is characterised by velvety, papillomatous, brownish-black, hyperkeratotic plaques, typically on the intertriginous areas and neck (1). AN commonly affects neck, axillae, groin, inner aspects of the thighs and is often routinely encountered in daily dermatological practice (2). Schwartz RA has classified AN into benign, obesity-associated, syndromic, malignancy-associated, 4unilateral, drug-induced, mixed-type and acral types (2). It is often associated with hyperinsulinemia, insulin resistance, benign endocrinopathies, heritable diseases and even malignancies (3). Histopathological findings characteristically show papillomatosis and hyperkeratosis (4).
Acral AN is more commonly seen in patients of African American descent. Acral AN (also known as acral acanthotic anomaly) and the lesions are usually localised to the knee, ankle, phalangeal joints and tarsophalangeal joints [5,6]. The occurrence of acral AN in Indian population is a rare phenomenon in itself and to the best of the author’s knowledge, the review of literature has revealed only two such cases from India [1,6]. One of the reported cases of acral AN in Indian population was of a 40-year-old female along with scleroderma and the other patient was a 28-year-old female without any other systemic involvement or endocrinopathy [1,6]. Although acral type of AN is not commonly associated with malignancy, recent case reports have demonstrated an association with gastric adenocarcinoma and Hodgkin’s lymphoma, thereby warranting a thorough workup of the patient (7),(8).
The exact aetiology of AN is unclear, but it is most commonly associated with insulin resistance. Increased circulating insulin leads to increase in circulating Insulin like Growth Factor (IGF) which causes keratinocyte and dermal fibroblast proliferation that is responsible for AN (9). Other factors that have been implicated in the pathogenesis of AN include obesity, endocrine dysfunction, malignancy, association with autoimmune diseases and medications such as systemic glucocorticoids, diethylstilbestrol, combined oral contraceptive pill, growth hormone therapy and oestrogen (10).
Diagnosis of AN is usually clinical and histopathology is rarely needed, for confirmation. However, the emergence of dermoscopy in the recent years has aided in providing a non invasive and accurate diagnostic tool for cases requiring further evaluation to confirm diagnosis, as in this case. Cutaneous pigmentation is one of the most strikingly variable phenotypes in humans, therefore making pigmentatory disorders manifest in a multitude of forms (11). This case presented only with asymptomatic hyperpigmented macules at acral sites which is not typical clinical picture of AN, however the dermoscopic findings of crista cutis and sulcus cutis led to the suspicion of acral AN. Common dermoscopy findings in AN are crista cutis, sulcus cutis, papillary projections, hyperpigmented dots, crypts, and blotching; which can all be correlated with histopathological features (4). This stresses the importance of dermoscopy as a non invasive diagnostic tool as skin biopsy is not a routine procedure for such cases.
Diagnostic work-up in patients of AN comprises of fasting lipid profile, fasting glucose, fasting insulin levels, haemoglobin, thyroid profile and radiological investigations (like chest X-ray PA view, ultrasonography whole abdomen and magnetic resonance imaging/computerised tomography) to rule out malignancy associated AN.
Treatment of AN is challenging and the mainstay of therapy aims at treating the underlying cause, such as controlling blood glucose levels through exercise and diet, treating the insulin resistance or treating the malignancy in cases of malignancy associated AN (12). AN associated with insulin resistance can be treated with drugs such as metformin and rosiglitazone which are insulin-sensitising agents (10).
Topical treatments include keratolytics, like topical retinoids, vitamin D3 analogues, urea and salicyclic acid. Physical modalities such as long pulsed alexandrite lasers, dermabrasion CO2 ablation and chemical peels have also been tried. All treatment methods have shown variable success (13).
Conclusion
The present case presented with hyperpigmented macules at acral sites instead of the routinely encountered plaques over flexures with concurrent serum vitamin B12 deficiency. This case is being reported due to its rare occurrence in the Indian population, the atypical clinical presentation in the form of macules, and to highlight dermoscopy as an essential non-invasive tool aiding in the diagnosis. The diagnosis of acral AN should not be overlooked despite the finding of low serum vitamin B12 levels in such a case, and the authors wish to create awareness among the clinicians to investigate the patient further.
Reference
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[ CrossRef] [ PubMed] | 8. | Song JY, Lim JH, Kim CW, Kim HO. A case of acral type acanthosis nigricans associated with lymphoma. Korean J Dermatology. 2002;841-43.
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[ CrossRef] [ PubMed] | 10. | Romo A, Benavides S. Treatment options in insulin resistance obesity-related acanthosis nigricans. Annals of Pharmacotherapy. 2008;42(7-8):1090-94.
[ CrossRef] [ PubMed] | 11. | Nouveau S, Agrawal D, Kohli M, Bernerd F, Misra N, Nayak CS. Skin hyperpigmentation in Indian population: Insights and best practice. Indian J Dermatol. 2016;61(5):487.
[ CrossRef] [ PubMed] | 12. | Patel NU, Roach C, Alinia H, Huang WW, Feldman SR. Current treatment options for acanthosis nigricans. Clin Cosmet Investig Dermatol. 2018;11:407-13.
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DOI: 10.7860/JCDR/2023/61029.17878
Date of Submission: Oct 23, 2022
Date of Peer Review: Dec 19, 2022
Date of Acceptance: Mar 11, 2023
Date of Publishing: May 01, 2023
AUTHOR DECLARATION:
• Financial or Other Competing Interests: None
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes
PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Nov 05, 2022
• Manual Googling: Feb 10, 2023
• iThenticate Software: Mar 06, 2023 (9%)
ETYMOLOGY: Author Origin
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