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Vol. 93. Núm. 5.
Páginas 740-742 (1 setembro 2018)
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Vol. 93. Núm. 5.
Páginas 740-742 (1 setembro 2018)
Open Access
Scanning electron microscopy of granuloma annulare*
Visitas
4405
Hiram Larangeira de Almeida Jr.1,2, Eduardo de Barros Coelho Bicca3, Mariani Magnus de Andrade4, Pedro da Rocha Andrade Neto4
1 Department of Dermatology, Universidade Federal de Pelotas, Pelotas (RS), Brazil.
2 Department of Dermatology, Universidade Católica de Pelotas, Pelotas (RS), Brazil.
3 Discipline of Pathology, Universidade Católica de Pelotas, Pelotas (RS), Brazil.
4 Medical student, Dermatology League, Universidade Federal de Pelotas, Pelotas (RS), Brazil.
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Abstract

Light microscopy of granuloma annulare shows mucin deposition with lympho-histiocytic infiltrate. We describe the ultrastructural three-dimensional aspects of a typical case of granuloma with characteristic histopathological findings. At the ultrastructural level, affected collagen bundles and granular mucin deposition were observed. Round cells corresponding to lymphocytes were identified. Bigger oval cells, corresponding to isolated or palisading histiocytes were also found. The ultrastructural aspects overlap with light microscopy and contribute to its iconographic documentation.

Keywords:
Histiocytes
Microscopy, electron, scanning
Mucins
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Introduction

Granuloma annulare (GA) is a well-known disease that was first described in 1895 by Thomas Colcott Fox. Henry Radcliffe Crocker, in 1902, coined the term granuloma annulare. It is a relatively common and benign lesion of unknown cause and consists of a granulomatous dermatitis, characterized by grouped papules in an enlarging annular shape. The disorder can affect people of any age or ethnicity. However, 66% of the patients are under 30 years of age, and it occurs more often in females than males.1,2

Localized GA occurs more often than the other forms, i.e., generalized or disseminated, perforating, and subcutaneous.2–4 The localized form of granuloma annulare corresponds to 75% of cases. It starts with a small ring of firm red or pink papules. As the condition progresses, there is some central involution, and then the ring slowly grows in diameter. The condition resolves within one to two years in 50% of the cases.5

Light microscopy of GA shows focal degeneration of collagen, with surrounding areas of reactive inflammation and fibrosis.2–5 The epidermis appears normal, except in the perforating variant. The pattern of collagen degeneration is a spectrum that varies from large foci of full degeneration, with surrounding palisaded histiocytes and central mucin, to small foci of incomplete collagen degeneration. An infiltration of lymphocytes, histiocytes and fibroblasts is found between the normal and partially degenerated collagen.6–8

We report a case of typical GA, which was biopsied for diagnosis confirmation (Figure 1). A small fragment of the dermis was separated for electron microscopy, fixed in glutaraldehyde, dehydrated, dried, metalized and examined with scanning electron microscopy (SEM). Light microscopy confirmed the clinical diagnosis, with granulomatous formation and dermal basophilic deposits associated with lymphohistiocytic infiltrate and some giant cells (Figure 2).

Figure 1.

Clinical aspect with typical annular lesion

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Figure 2.

Light microscopy. A - basophilic mucin deposition, histiocytes and multinucleated giant cells (Hematoxylin & eosin, x200). B - disorganized collagen bundles (Hematoxylin & eosin, x200)

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Results

Ultrastructural examination demonstrated normal collagen fibers arranged in parallel distribution, forming bundles (Figure 3A). In some examined fields, adjacent to the normal collagen, granular deposits corresponding to mucin deposition were observed amid irregular collagen that lacked bundle formation (Figure 3B and 3C). Some round cells corresponding to lymphocytes were seen (Figure 3D). Some fields showed important collagen compaction (Figure 4A), where individual collagen fibers/bundles were no longer identified. Large oval-shaped cells corresponding to histiocytes were found alone (Figure 4B), forming palisade arrangements (Figure 4C), or even in groups (Figure 4D).

Figure 3.

Scanning electron microscopy. A - normal collagen bundles in the lesion’s border (x1,500). B - granular deposition of mucin and collagen fibers without bundle formation (x8,000). C - detail of granular mucin deposition (x10,000). D - detail of the compaction of the collagen by granular mucin deposition with two inflammatory lymphocytes (x10,000)

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Figure 4.

Scanning electron microscopy. A - Strong compaction of dermal collagen. (x1,500); B - isolated histiocyte with a lymphocyte to the left (x7,000); C - detail of an area with significant compaction of collagen, with palisading histiocytes (x5,000); D - grouped histiocytes (x6,000)

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Discussion

The only publications on ultrastructural analysis of GA used transmission electron microscopy. These studies reported degeneration of elastic fibers, under phagocytic stimulation by macrophages and giant cells.9,10 Elastic fibers and collagen around the granulomas are within normal limits.10 The normally well-defined collagen bundles had disintegrated, and the regular parallel arrangement of the single fibrils within the bundles was lost.

The fibrils were swollen, cross-striated and degenerate into a granular and amorphous material.10 Histiocytes were predominant; monocytes, giant epithelioid cells and fibroblasts were also found.

Granuloma annulare observed in scanning electron microscopy has not been reported in the medical literature.

Therefore, we conclude that the findings of the scanning electron microscopy overlap with the findings of optical microscopy, allowing three-dimensional iconographic documentation of this well-known dermatosis. The reported collagen “degeneration” in light microscopy is probably due to the tight compaction of collagen because of mucin deposition, as seen with SEM, corresponding to the disorganized collagen fibers in previous reports using transmission electron microscopy.

Financial support: None.

Conflict of interest: None.

References
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[2.]
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Am J Dermatopathol., 8 (1986), pp. 302-308

Work conducted in the Postgraduate Program of Health and Behavior, Universidade Católica de Pelotas, Pelotas (RS), Brasil; Dermatology League, Universidade Federal de Pelotas, Pelotas (RS), Brasil.

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