Congenital giant lower eyelid hidrocystoma in a patient with possible orofacial digital syndrome: case report and literature review
Dimitriοs DELIGIANNIDIS, Dimitris TATSIS, Despoina MICHAILIDOU, Nikoleta PASTELLI, Konstantinos ANTONIADES
Department of Oral and Maxillofacial Surgery, General Hospital G. Papanikolaou (Head: Prof K. Antoniades)
Hellenic Archives of Oral & Maxillofacial Surgery (2021) 1, 5-11
SUMMARY: Hidrocystomas are benign cystic lesions which arise from the secretory part of sweat glands. Hidrocystomas can be either eccrine or apocrine and are often found in the head and neck region. In this paper we present a case of a large congenital hidrocystoma of the lower eyelid in a patient with possible orofacial digital syndrome (ODS). A special feature in our case was the presentation of bone remodeling of the anterior surface of the maxilla. The basic clinical and histological features of hidrocystomas are also reviewed.
KEY WORDS: Hidrocystoma, eyelid, syndactyly.
REFERENCES
Al Rasheed R, Al Samnan M. Congenital giant orbital eccrine hidrocystoma. Am J Ophthalmol Case Rep. 2019 Dec; 16: 100570
Alagheband M., Maida M.F. Asymptomatic periorbital, bluish cystic papule. Cortl Forum. 2004 Jan;17(1):36–41
Alfadley A, Al Aboud K, Tulba A, Mazen M. Multiple eccrine hidrocystomas of the face. Int J Dermatol. 2001;40:125–129
De Viragh PA, Szeimies RM, Eckert F. Apocrine cystadenoma, apocrine hidrocystoma, and eccrine hidrocystoma: three distinct tumors defined by expression of keratins and human milk fat globulin 1. J CutanPathol 1997: 24: 249-255
Deprez M, Uffer S. Clinicopathological features of eyelid skin tumors. A retrospective study of 5504 cases and review of literature. Am J Dermatopathol 2009;31(3):256 –262.
Font RL. Ophthalmic Pathology. An Atlas and Textbook. 3rd ed. Philadelphia: WB Saunders; 1996. Eyelids and lacrimal drainage system; pp. 2229–32.
Gurrieri F, Franco B, Toriello H, Neri G. Oral-facial-digital syndromes: review and diagnostic guidelines. Am J Med Genet A 2007 Dec 15;143A(24):3314-23
Hampton PJ, Angus B, Carmichael AJ. A case of Schopf-Schulz-Passarge syndrome. ClinExpDermatol 2005;30(5): 528–530.
Holder WR, Smith JD, Mocega EE. Giant apocrine hidrocystoma. Arch Dermatol. 1971;104(5):522-3
JakobiecF, Zakka F. A reappraisal of eyelid eccrine and apocrine hidrocystomas: microanatomic and immunohistochemical studies of 40 lesions. Am J Ophthalmol.2011 Feb;151(2):358-74.e2.
Mehrdad Malihi, Roger E. Turbin, Neena Mirani& Paul D. Langer. Giant Orbital Hydrocystoma in Children: Case Series and Review of the Literature, Orbit2015, 34:5,292-296
Sangueza OP, Cassarino DS, Glusac EJ, Kazakov DV, Requena L, Swanson PE, Vassalo C. WHO Classification of Skin Tumours. 4th ed. Chapter 3, p.183. IARC, Lyon, 2018
Sarabi K, Khachemoune A.Hidrocystomas - a brief review. Med Gen Med 8(3):57, 2006
Singh M, Kaur M, Gautam N. Giant eccrine hidrocystoma of the eyelid. Indian J Dermatol Venereol Leprol 2017;83:267
Temple IK, MacDowall P, Baraitser M, Atherton DJ. Focal dermal hypoplasia (Goltz syndrome). J Med Genet 1990; 27(3):180–187.
Warwick R, Williams PL .Gray's Anatomy, 35th ed. Longman Group Ltd: Edinburgh, 1973, pp 1168–1169
Department of Oral and Maxillofacial Surgery, General Hospital G. Papanikolaou (Head: Prof K. Antoniades)
Hellenic Archives of Oral & Maxillofacial Surgery (2021) 1, 5-11
SUMMARY: Hidrocystomas are benign cystic lesions which arise from the secretory part of sweat glands. Hidrocystomas can be either eccrine or apocrine and are often found in the head and neck region. In this paper we present a case of a large congenital hidrocystoma of the lower eyelid in a patient with possible orofacial digital syndrome (ODS). A special feature in our case was the presentation of bone remodeling of the anterior surface of the maxilla. The basic clinical and histological features of hidrocystomas are also reviewed.
KEY WORDS: Hidrocystoma, eyelid, syndactyly.
REFERENCES
Al Rasheed R, Al Samnan M. Congenital giant orbital eccrine hidrocystoma. Am J Ophthalmol Case Rep. 2019 Dec; 16: 100570
Alagheband M., Maida M.F. Asymptomatic periorbital, bluish cystic papule. Cortl Forum. 2004 Jan;17(1):36–41
Alfadley A, Al Aboud K, Tulba A, Mazen M. Multiple eccrine hidrocystomas of the face. Int J Dermatol. 2001;40:125–129
De Viragh PA, Szeimies RM, Eckert F. Apocrine cystadenoma, apocrine hidrocystoma, and eccrine hidrocystoma: three distinct tumors defined by expression of keratins and human milk fat globulin 1. J CutanPathol 1997: 24: 249-255
Deprez M, Uffer S. Clinicopathological features of eyelid skin tumors. A retrospective study of 5504 cases and review of literature. Am J Dermatopathol 2009;31(3):256 –262.
Font RL. Ophthalmic Pathology. An Atlas and Textbook. 3rd ed. Philadelphia: WB Saunders; 1996. Eyelids and lacrimal drainage system; pp. 2229–32.
Gurrieri F, Franco B, Toriello H, Neri G. Oral-facial-digital syndromes: review and diagnostic guidelines. Am J Med Genet A 2007 Dec 15;143A(24):3314-23
Hampton PJ, Angus B, Carmichael AJ. A case of Schopf-Schulz-Passarge syndrome. ClinExpDermatol 2005;30(5): 528–530.
Holder WR, Smith JD, Mocega EE. Giant apocrine hidrocystoma. Arch Dermatol. 1971;104(5):522-3
JakobiecF, Zakka F. A reappraisal of eyelid eccrine and apocrine hidrocystomas: microanatomic and immunohistochemical studies of 40 lesions. Am J Ophthalmol.2011 Feb;151(2):358-74.e2.
Mehrdad Malihi, Roger E. Turbin, Neena Mirani& Paul D. Langer. Giant Orbital Hydrocystoma in Children: Case Series and Review of the Literature, Orbit2015, 34:5,292-296
Sangueza OP, Cassarino DS, Glusac EJ, Kazakov DV, Requena L, Swanson PE, Vassalo C. WHO Classification of Skin Tumours. 4th ed. Chapter 3, p.183. IARC, Lyon, 2018
Sarabi K, Khachemoune A.Hidrocystomas - a brief review. Med Gen Med 8(3):57, 2006
Singh M, Kaur M, Gautam N. Giant eccrine hidrocystoma of the eyelid. Indian J Dermatol Venereol Leprol 2017;83:267
Temple IK, MacDowall P, Baraitser M, Atherton DJ. Focal dermal hypoplasia (Goltz syndrome). J Med Genet 1990; 27(3):180–187.
Warwick R, Williams PL .Gray's Anatomy, 35th ed. Longman Group Ltd: Edinburgh, 1973, pp 1168–1169
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