|
|
| Year : 2022 | Volume
: 15
| Issue : 2 | Page : 199-201 |
|
| Dermoscopic clues to syringocystadenoma papilliferum |
|
|
Gargi Taneja1, Aditi Dhanta1, Michael Leonard Anthony2, Neirita Hazarika1
1 Department of Dermatology, Venereology, and Leprology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand 249203, India
2 Department of Pathology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand 249203, India
Click here for correspondence address and email
| Date of Web Publication | 21-Jul-2022 |
|
|
 |
|
How to cite this article:
Taneja G, Dhanta A, Anthony ML, Hazarika N. Dermoscopic clues to syringocystadenoma papilliferum. J Cutan Aesthet Surg 2022;15:199-201 |
 Case Presentation | |  |
A 16-year-old male presented with multiple lesions on the left side of face present since birth. The lesions were asymptomatic and increasing in size since past 2–3 years. History of occasional discharge and bleeding from the lesions was present. There was no other complaint and family history was negative. General and systemic examination was within normal limits. Cutaneous examination revealed multiple grouped red to brown, dome-shaped, firm nodules and plaques with erosions and crusting over the surface present on the left pre-auricular area. Few lesions had central umbilication [Figure 1]. Dermoscopy done on an umbilicated nodule (marked with black arrow in [Figure 1]) using a hand-held dermoscope (DermLite 3Gen, in 10× magnification in polarized mode) revealed multiple bluish-white and reddish-white areas in background with central umbilication and polymorphic vessels. Yellowish areas representing crusting and whitish scales were also seen [Figure 2]. A 4-mm punch biopsy was performed on a representative lesion on the left side face. Histological examination revealed multiple papillary projections and cystic invaginations present in the upper dermis (H&E, 4×) [Figure 3]. On high power (H&E, 40×), papillary projections were lined by two rows of cells with inner row of high columnar cells having oval nuclei and faint eosinophilic cytoplasm and outer row having small cuboidal cells with round nuclei and scanty cytoplasm. Also, lymphoplasmacytic infiltrate was also present in the core of the papillary projections [Figure 4]. | Figure 1: Multiple grouped red to brown, dome-shaped, firm nodules and plaques with erosions and crusting over the surface present on the left pre-auricular area. Few lesions had central umbilication. Black arrow marks area where dermoscopy was performed
Click here to view |
 | Figure 2: Multiple bluish-white and reddish-white areas in background (black circles) with central umbilication (blue arrow) and polymorphic vessels (black arrow). Yellowish areas representing crusting (red arrow) and whitish scales (green arrow) were present (DermLite 3Gen, 10×, polarized mode)
Click here to view |
 | Figure 3: Multiple papillary projections and cystic invaginations present in the upper dermis (H&E, 4×)
Click here to view |
 | Figure 4: Papillary projections in the upper dermis lined by two rows of cells with inner row of high columnar cells having oval nuclei and faint eosinophilic cytoplasm and outer row having small cuboidal cells with round nuclei and scanty cytoplasm. Mild lymphoplasmacytic infiltrate was present in the core of papillary projections (H&E, 40×)
Click here to view |
Based on history, clinical, dermoscopic, and histological examination, a diagnosis of syringocystadenoma papilliferum (SCAP) was made and the patient was referred to a plastic surgeon for excision of lesion.
| Discussion | | |
SCAP is a rare, benign, hamartomatous, adnexal tumor which arises from pluripotent cells exhibiting eccrine or apocrine lineage. Apocrine origin is more favored. About 50% of the cases are present at birth and up to 15–30% of the cases are seen at puberty.[1] The most frequent location is the head and neck, with scalp being the preferred location. It may present as three common types: plaque type, solitary nodular type, and linear type. Plaque type is commonly present on scalp which enlarges during puberty to become nodular, verrucous, or crusted. Linear type presents as multiple reddish pink firm papules or umbilicated nodules commonly occurring over face and neck. Solitary nodular type, in contrast, presents as nodules with predilection for the trunk, shoulder, and axillae.[2] The present case is a combination of plaque and linear type of SCAP.
SCAP is known to be associated with other benign neoplasms such as sebaceous nevus of Jadassohn, apocrine adenoma, hidradenoma papilliferum, trichoblastoma, and others.[3] Association of SCAP with basal cell carcinoma is seen in up to 10% of the cases. Histopathologically, it presents as irregular papillary projections of scaly epithelium, forming ductile structures, aligned by glandular epithelium formed by an external layer of cuboid cells, with round nuclei and scarce cytoplasm, and an internal layer of cylindrical cells with decapitation secretion and plasmacyte-rich inflammatory infiltrate.[4] Tumor cells stain positive for carcinoembryonic antigen. Dermoscopic findings in SCAP include milky red papillomatous projections with a central ulceration or crater. Polymorphic vessels can be appreciated within the darker ulcerated areas.[5] We noted multiple, bluish-white to reddish-white, structureless areas with central umbilication and polymorphic vessels. Whitish scaling and yellowish crusting were also noted in our patient. The central crater noted on dermoscopy corresponded to the characteristic cystic invagination in histopathology, whereas the white structureless area represented the surrounding hyperplastic epidermis.[6]
Dermoscopy can help play an important role in clinching the diagnosis. The dermoscopic findings of syringocystadenoma papilliferum and its differentials are summarized in [Table 1].[5],[6] Treatment options of SCAP include surgical excision or ablation with CO2 laser.
In conclusion, SCAP is an uncommon tumor in the head and neck area in the pediatric age group, which may rarely undergo malignant transformation. Early diagnosis and removal of the lesion are crucial.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| References | | |
| 1. | Böni R, Xin H, Hohl D, Panizzon R, Burg G. Syringocystadenoma papilliferum. A study of potential tumor suppressor genes. Am J Dermatopathol 2001;23:87-9.  |
| 2. | Pinkus H Life history of naevus syringocystadenomatous papilliferus. Arch Dermatol Syphil 1954;69:305-22. |
| 3. | Kar M, Kar JK, Maiti S Giant linear syringocystadenoma papilliferum of the back. Indian J Dermatol Venereol Leprol 2012;78:123. |
| 4. | Bruno CB, Cordeiro FN, Soares Fdo E, Takano GH, Mendes LS Dermoscopic aspects of syringocystadenoma papilliferum associated with nevus sebaceus. An Bras Dermatol 2011;86:1213-6. |
| 5. | Chauhan P, Chauhan RK, Upadhyaya A, Kishore S Dermoscopy of a rare case of linear syringocystadenoma papilliferum with review of the literature. Dermatol Pract Concept 2018;8:33-8. |
| 6. | Dash S, Nayak AK, Sethy M, Palit A, Behera B Dermoscopic findings of de novo syringocystadenoma papilliferum. Indian J Dermatol Venereol Leprol 2021;87:278-80. |
Correspondence Address:
Neirita Hazarika
Department of Dermatology, Venereology, and Leprology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand 249203
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/JCAS.JCAS_103_21
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1] |
|
|
|
|
|
|
|
|
|
|
|
|
|
| Article Access Statistics | | | Viewed | 140 | | | Printed | 2 | | | Emailed | 0 | | | PDF Downloaded | 7 | | | Comments | [Add] | | |
|
|
