Coexistence of Riehl's Melanosis, Lupus Erythematosus and Thyroiditis in a Patient.

Introduction: Riehl's melanosis (RM) is an acquired hyperpigmentation disorder, presenting diffused and reticulate brownish-gray pigmentation, preferentially on the face and neck. RM overlaps with systemic lupus erythematosus (SLE) and Hashimoto's thyroiditis has never been reported. Case: We report a case of RM patient accompanied with SLE and Hashimoto's thyroiditis of primary hypothyroidism. Progressing, diffuse, symmetric, and reticular hyperpigmentation was seen on the face, neck, and upper limbs, manifesting as typical melanosis. Skin microscopy showed diffuse black-pepper-like changes and telangiectasias. The diagnosis of SLE and primary hypothyroidism were confirmed by follow-up investigations. The hyperpigmentation turned notably lighter after 14 months of treatment with prednisone, hydroxychloroquine, and L-thyroxine. Discussion: The exact pathogenesis of RM is unclear and exposure to coal tar dyes, ultraviolet, and fragrance fixatives in cosmetics are believed to be contributing factors, while some cases involve no triggers. It is not impossible that RM is a rare skin manifestation of SLE that has never been reported. The skin hyperpigmentation in this patient was not triggered by thyroid disease.
Conclusion: RM could be a skin manifestation of autoimmunity. Coexistence of RM, lupus erythematosus and thyroiditis in the same patient is rare and has never been reported.

Introduction

Autoimmune diseases are a series of diseases caused by morbid immune reactions. Coexistence of autoimmune diseases is common. Systemic lupus erythematosus (SLE)-associated Hashimoto’s thyroiditis has been reported up to 12.6% of the cases.1 Riehl’s melanosis (RM) is an acquired hyperpigmentation disorder, presenting diffused and reticulate brownish-gray pigmentation, preferentially on the face and neck, and the histopathological features include basal cell liquefactive degeneration, dermal melanin incontinence and/or lymphohistiocytic infiltrate, and upper dermal melanophage infiltration.2 RM overlaps with SLE and Hashimoto’s thyroiditis has never been reported.

Case

History

A 30-year-old Chinese woman came to the dermatology clinic with a two-year history of progressing, diffuse, lattice-like hyperpigmentation of the face and neck. Significant sunlight, chemical materials, medicine, and cosmetic exposures were denied. She had no notable family history of similar conditions. On further questioning, she admitted that she had experienced hair loss and ankle joint pain for two years, and these had worsened in the last two months.

Physical Examination

Diffuse, symmetric, and reticular gray brown hyperpigmentation was observed all over the face and neck, especially the cheeks and the area around the mouth (Figure 1A–C). Slight hyperpigmentation was seen on her upper limbs. No similar change can be seen on the rest of her skin and mucosa.

Figure 1

Clinical features of the patient before and after treatment. (A–C). Clinical features of the patient before treatment. Diffuse, symmetric, and reticular gray brown hyperpigmentation on the face and neck. (D–F). Clinical features of the patient after treatment. The hyperpigmentation on the face and neck turn much lighter.

Investigation

Under skin microscopy, diffuse black-pepper-like changes separated by hair follicles with sweat glands and telangiectasias were seen (Figure 2A). The reflectance confocal microscopy showed abundant melanin in the epidermis and dermis, local liquefactive degeneration of basal layer cells, and the presence of melanophages in the dermis (Figure 2C and D). Histopathology of neck lesions (HE staining) showed punctiform epidermal atrophy, punctate liquefactive degeneration of basal layer cells, melanophages in the dermis, and a few lymphocytes infiltrating around the dermal adnexa (Figure 3A). Masson-Fontana silver staining showed amounts of melanin in the epidermis and dermis (Figure 3B). Laboratory investigations revealed the following: peripheral white blood cell (WBC) count 2.73 × 109/L (3.5–9.5 × 109/L), antinuclear antibody (ANA) (+++), anti-dsDNA antibody (dsDNA) (+), anti-Sjögren’s-syndrome-related antigen antibody A (+++), C3 0.48 g/L (0.90–1.80 g/L), C4 0.06 g/L (0.10–0.40 g/L), anti-thyroglobulin antibody (TGAb) >4000 IU/mL (0.00–115.00 IU/mL), and anti-thyroid peroxidase (ATPO) >600 IU/mL (0.00–34.00 IU/mL), thyroid stimulating hormone (TSH) 92 mIU/L (0.550–4.780 mIU/L), Thyronine-4 (T4) 2.5 μg/dl (4.5–10.9 μg/dl). Serum-free thyroxine (FT4), free triiodothyronine (FT3), thyronine-3 (T3), and adrenocorticotrophic hormone (ACTH) were all within normal range. Anti-TSH receptor antibody (TRab) was negative. Doppler ultrasonography of the thyroid showed hypothyroidism changes and a nodular thyroid cyst. Serum sex hormone, adrenal hormone, and the computed tomography scanning of the adrenal glands were all normal.

Figure 2

Dermoscopic and reflectance confocal microscopy features before and after treatment. (A). Dermoscopic features of the patient before treatment. Diffuse black-pepper-like changes separated by hair follicles with sweat glands and telangiectasias can be seen. (B). Dermoscopic features of the patient after treatment.The hyperpigmentation turn much lighter. (C and D). Reflectance confocal microscopy features of basal layer and dermis before treatment. Abundant melanin in the epidermis and dermis, local liquefactive degeneration of basal layer cells, and the presence of melanophages in the dermis. (E). Reflectance confocal microscopy feature of basal layer after treatment. The melanin in the epidermis decrease significantly, the local liquefactive degeneration of basal layer cells show improvement, and the melanophages in dermis decrease in number.

Figure 3

Histopathologic features. (A). Histopathology of neck lesions show punctiform epidermal atrophy, punctate liquefactive degeneration of basal layer cells, melanophages in the dermis, and a few lymphocytes infiltrating around the dermal adnexa (HE staining, x100, bar=200μm). (B). A large amount of melanin in the epidermis and dermis (Masson-Fontana silver staining, x100, bar=200 μm).

Diagnosis

Diagnoses of RM accompanied with SLE and Hashimoto’s thyroiditis of primary hypothyroidism were made via the clinical features and laboratory investigations.

Treatment

Prednisone (20 mg/day), hydroxychloroquine (400 mg/day), and L-thyroxine (100 μg/day) were administered orally. The prednisone was withdrawn gradually over the course of 7 months.

Follow-Up

Significant improvement was observed after 14 months of treatment. The hyperpigmentation has turned much lighter (Figures 1D–F and 2B). Under reflectance confocal microscopy, the melanin in the epidermis was found to have decreased significantly, the local liquefactive degeneration of basal layer cells showed improvement, and the melanophages in dermis was found to have decreased in number (Figure 2E). WBC, C3, C4, and T4 returned to normal. The TSH decreased to 5.667 mIU/L.

Discussion

The exact pathogenesis of RM is unclear and exposure to coal tar dyes, ultraviolet (UV), and fragrance fixatives in cosmetics are believed to be contributing factors, while some cases involve no triggers.2 In this patient, clinical and histological features confirmed the diagnosis of RM. Significant sunlight, chemical materials, medicine, and cosmetic exposures were denied. The hyperpigmentation is not likely caused by contact elements. Hyperpigmentation after inflammation was excluded for those without a history or accompanied with erythema and edema. Liquefactive degeneration of basal layer cells can be seen in cutaneous lupus erythematosus (CLE) as well, but increased melanin in the epidermis and melanophages in the dermis are rare. Pigment changes in CLE are usually post-inflammatory hyperpigmentation and are not common. Acute cutaneous lupus erythematosus (ACLE) usually leaves transient pigmentary changes, especially in dark-skinned people.3 The concurrent onset of hyperpigmentation and symptoms of SLE in this patient, as well as their improvement during treatment for SLE suggest an association. It is not impossible that RM is a rare skin manifestation of SLE that has never been reported. Recently, Calleja et al4 and Azrielant et al5 reported six and three LE patients who presented facial pigmentation, respectively. The hyperpigmentation of these patients is mostly isolated, limited in the face, and accompanied with erythema, which is different from the lesion of the present patient and not consistent with the diagnosis of melanosis. Miyoshi et al6 and Takeo et al7 have reported several patients with Sjogren’s syndrome who had Riehl’s melanosis-like eruption associated with anti-SSA (Ro) positive. In this case, anti-SSA was positive as well, implying this autoantibody plays a role in the development of hyperpigmentation in autoimmune diseases.

Song8 reported a case in which a 42-year-old Chinese woman with Graves’ disease developed general hyperpigmentation. T4, ACTH, and TRab were elevated. The elevation of ACTH and TRab was found to stimulate the production of cAMP, promoting the proliferation and differentiation of melanocytes, resulting in hyperpigmentation of skin. In the present case, FT4 and ACTH were within normal range, and the TRab was negative. Serum adrenal hormones, sex hormones, and blood glucose were all within normal ranges, and the results of adrenal computed tomography scanning were negative, and type II polyglandular autoimmune syndrome was excluded, which could cause hyperpigmentation as skin damage.9 This suggests that skin hyperpigmentation in this patient was not triggered by thyroid disease.

Conclusion

The exact pathogenesis of RM is not clear, and it could be a skin manifestation of autoimmunity. RM overlaps with SLE and Hashimoto’s thyroiditis has never been reported before.