Nevus lipomatosus superficialis

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Nevus lipomatosus superficialis
Other namesNevus lipomatosis of Hoffman and Zurhelle
SpecialtyDermatology

Nevus lipomatosus superficialis (NLS or NLCS, also known as nevus lipomatosis of Hoffman and Zurhelle

plaques, usually of the buttock or thigh, less often of the ear or scalp, with a wrinkled rather than warty surface.[1][2]
: 625  It is usually congenital in origin or appears within the first three decades.[3]

A pedunculated lipofibroma is a solitary variant of nevus lipomatosus superficialis. It usually appears in adult life, and usually on the axilla, knee, ear, arm, scalp and the lower trunk.[3]

In both multiple and solitary variants, the

fibroepithelioma of Pinkus.[3]

Signs and symptoms

Clinically, there are two variations. The most prevalent variety, known as the classical type, is characterized by a number of flesh-colored or yellowish sessile lesions that have a propensity to combine into smooth or cerebriform plaques that are distributed linearly, zosteriformly, or segmentally. Lessons tend to focus on the lower trunk, particularly the gluteal, sacrum, and lumbar regions as well as the

The second clinical pattern of NLCS is a solitary papule or nodule that typically appears later in life. It mimics a skin tag in appearance and is flesh-colored and domed. The solitary form, which has been reported on the arms, knees, ears, axillae, nose, calves, clitoris, and scalp, has no known specific distribution.[5][6][7]

The lesions are asymptomatic in both forms.[8] In rare cases, ulceration happens, particularly following ischemia or external damage.[9] Moreover, coexisting comedo-like changes, leukodermic patches, café-au-lait macules, and overlaying hypertrichosis are possible.[10][11]

Causes

Although the pathophysiology of NLCS is unknown, ectopic adipocytes may arise from pericytes, similar to embryonic lipogenesis, or from precursor cells from the dermal arteries.[12][13]

Diagnosis

The histology of NLCS typically demonstrates the proliferation of ectopic mature

Acanthosis, basket weave hyperkeratosis, elevated basal pigmentation, and obliteration with focal rete ridge extension are observed in the epidermis.[8] Adnexal structures may exhibit perifollicular fibrosis and be unaffected or diminished in certain instances.[13]

Clinically, NLCS needs to be distinguished from focal dermal hypoplasia (Goltz syndrome), neurofibroma, lymphangioma, hemangioma, sebaceous nevus, and connective tissue nevus.[9][11]

Treatment

Given the rarity of malignant degeneration and systemic problems, treatment is only recommended for cosmetic reasons.[10] The best course of treatment is surgical excision because recurrence lesions are uncommon.[11]

See also

  • Skin lesion
  • List of cutaneous conditions

References

Further reading

External links