Syringocystadenoma Papilliferum and Nevus Sebaceus (Jadassohn) Occurring as a Single Tumor

Grund, J. L.

doi:10.1001/archderm.1952.01530220081008

Cited by 10 publications

(2 citation statements)

References 8 publications

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“…We also have been able to confirm the carlior obsorvations,* of a close aR.sociation between s\Tingocyatadeiiorna i»apilliferum and naevus sebuceus. Our figure of 27 .syringocystadenoniata • Arzt and Kumer (1925);DiirfFel (1935); Percival {1947}; Marcus and Wooldridge (1950); Grund and F-.lan (1951); Grund (1952);Pinkus (1954); Hplwig and Hackney (1055) Habor (1955); Wittig (iy;")O); Castolain and Spitalier (1!I5')); Wuringer (1960);Micbalow.ski (1962). in 140 naevi is rather higher than the IS out of 150 found by Mehregan and Pinkus; this may reflect the rather higher ages of our patients, 86 of whoni were aged 20 or over, as compared with 6S over the age of 18 in the aeries of Meiiregan and Pinkus. Our figures for the incidence of apocrine glands aud of sebaceous gland changes were also roughly similar.…”

Section: Discussionmentioning

confidence: 92%

Naevus Sebaceus.

1970

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SUMMARY.— The clinical records and the histopathology of 140 cases of naevus sebaceus and related compound epidermal naevi have been studied with special reference to the incidence of secondary tumours. In 27 lesions there were areas of syringocystadenoma papilliferum, sometimes forming a large part of the naevus. In 9 lesions, basal cell epithelioma was a secondary development, but only 3 of these epitheliomata showed evidence of an aggressive growth pattern. Fourteen other naevi were found histologically to have small areas of basaloid proliferation, but these proliferations were considered to be harnartomatous rather than epitheliomatous in nature. So far, on follow‐up, none of the basal cell epitheliomata has recurred after treatment. A rare complication found in a patient aged 56 was the development of a squamous cell epithelioma which, although poorly differentiated, had not recurred 4 years after excision. Other related lesions were 3 syringomata, 2 apocrine cystadenomata and 2 osteomata. Some of the naevi showed areas of unusual squamous proliferation which were difficult to categorize histologically; in 2 instances keratoacanthomata were simulated; other proliferations showed “clear cell” differentiation or pseudo‐epitheliomatous hyperplasia. It was concluded from this study that there is only a small risk of a serious malignant tumour supervening in naevus sebaceus, and that simple surgical excision is usually adequate treatment.

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Section: Discussionmentioning

confidence: 92%

Naevus Sebaceus.

1970

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“…And SP and nevus sebaceous are considered to share the same origin from the primary epithelial-germ. Apocrine differentiation of the germ cells leads SP, though not as well-differentiated as in sebaceous nevus [8]. And sebaceous nevus is known as an origin of many kinds of benign and malignant neoplasms including SCC [9].…”

Section: Discussionmentioning

confidence: 99%

A Case of Giant Squamous Cell Carcinoma of the Buttock Possibly Arose from Syringocystadenoma and Invaded to the Rectum

Nishioka

Tanemura

Yamanaka

et al. 2011

Journal of Skin Cancer

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We report a rare case of giant squamous cell carcinoma of the buttock infiltrated to the rectum. The tumor may have arisen from syringocystadenoma papilliferum. Since there was no sign of metastasis, radical operation including rectal amputation was performed after successful neoadjuvant therapies. Afterwards, the patient has been alive free from disease for 15 months with no lymph node and distant organ metastasis.

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Life History of Naevus Syringadenomatosus Papilliferus

Pinkus¹

1954

Arch Dermatol

114

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Syringocystadenoma Papilliferum and Nevus Sebaceus (Jadassohn) Occurring as a Single Tumor

Cited by 10 publications

References 8 publications

Naevus Sebaceus.

Naevus Sebaceus.

A Case of Giant Squamous Cell Carcinoma of the Buttock Possibly Arose from Syringocystadenoma and Invaded to the Rectum

Life History of Naevus Syringadenomatosus Papilliferus

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