Letters to the Editor
and breakdown of skin overlyinging a contiguous tubercular focus in a person with low immunity and tuberculosis verrucosa cutis, an exogenous and paucibacillary form occurring after accidental superinfection or autoinoculation or post‑traumatic inoculation with infected sputum occurring in a person with good immunity.[1] Coexistence of these types of cutaneous tuberculosis with tuberculosis verrucosa cutis developing after scrofuloderma in nearby skin was reported previously by Sethuraman et al.,[3]. Müzeyyen et al.,[2] reported a case where tuberculosis verrucosa cutis was located distant from scrofuloderma. Tuberculosis verrucosa cutis coexisting with articular tuberculosis was reported by Marquet et al.,[6] while scrofuloderma overlying the acromio‑clavicular joint was reported by Tan et al.[7] In our patient, two lesions of tuberculosis verrucosa cutis and two lesions of scrofuloderma with underlying joint involvement were seen in different areas of the hands and feet. The co‑existence of multifocal cutaneous tuberculosis of different forms with joint involvement is rare.
Neelakantababu Rasineni, P. Venkata Ramana, Sridevi Kota, Ramesh Kumar Gandikota Department of Dermatology, Venereology and Leprology, Sri Venkateswara Ramnarayan Ruia Government General Hospital, Sri Venkateswara Medical College, Tirupathi, Andhra Pradesh, India Address for correspondence: Dr. Neelakantababu Rasineni, Department of Dermatology, Venereology and Leprology, Sri Venkateswara Ramnarayan Ruia Government General Hospital, Sri Venkateswara Medical College, Tirupathi ‑ 517507, Andhra Pradesh, India. E‑mail: [email protected]
REFERENCES: 1.
2. 3. 4. 5.
Sethi A.Tuberculosis and infections with atypical mycobacteria. In: Goldsmith LA, Katz SI, Gilcherst BA, Paller AS, Leffell DJ, Wolff K, editors. Fitzpatrick’s Dermatology in General Medicine. 8th ed. New York: McGraw‑Hill; 2012. p. 1225‑36. Gönül M, Gül U, Kilic A, Soylu S, Demiriz M, Kubar A. Coexistence of tuberculosis verrucosa cutis with scrofuloderma. Turk J Med Sci 2008;38:495‑9. Sethuraman G, Kaur J, Nag HL, Khaitan BK, Sharma VK, Singh MK. Symmetrical scrofuloderma with tuberculosis verrucosa cutis. Clin Exp Dermatol 2006;31:475‑7. Rajan J, Mathai AT, Prasad PV, Kaviarasan PK. Multifocal tuberculosis verrucosa cutis. Indian J Dermatol 2011;56:332‑4. Martinez SF, Mihalko MJ. Tuberculosis and other unusual infections. In: Canale ST, Beaty JH, editors. Campbell’s Operative Orthopaedics. 11th ed. Philadelphia: Mosby Company; 2008. p. 753‑71.
6. Marquet A, Moya L, Aldanondo I, Muñoz‑Zato E, Carrillo R, Jaén P. Coexistence of tuberculosis verrucosa cutis and articular tuberculosis in the same patient. Actas Dermosifiliogr 2006;97:56‑8. 7. Tan WP, Tang MB, Tan HH. Scrofuloderma from the acromioclavicular joint presenting as a chronic ulcer in an immunocompetent host. Singapore Med J 2007;48:e243‑5. Access this article online Quick Response Code:
Website: www.ijdvl.com DOI: 10.4103/0378-6323.136921 PMID: *****
Severely disfiguring multiple familial trichoepitheliomas with basal cell carcinoma Sir, Trichoepitheliomas are benign adnexal neoplasms that originate from hair follicles. It can present as solitary non‑familial or multiple familial forms. Multiple familial trichoepitheliomas is an autosomal dominant disorder characterized by numerous nodules and papules predominantly on the face and occasionally on the scalp.[1] Herein, we describe a rare case of this condition, with severe facial disfigurement, involving 6 members of a family in three generations. In the oldest affected member, one of the lesions evolved into a basal cell carcinoma. A 55‑year‑old, rural housewife of Arabian descent presented with slowly progressive facial skin lesions since 37 years. She had noticed her skin lesions at the age of 18 years and they gradually increased in size and number. Although she had sought no medical advice for her asymptomatic lesions during these years (due to her low socio‑economic status), her disfigured face resulted in social isolation. As one of her skin lesions became pruritic and ulcerated recently, she sought medical attention. Physical examination revealed numerous painless, round‑to‑oval, discrete and/or confluent, soft and firm, skin‑colored or pinkish, papules and nodules ranging from 1 to 5 cm in size. These lesions covered the whole face but were predominantly clustered on her peri‑nasal and chin
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
349
Letters to the Editor
a
b
Figure 2: Biopsy of the lesion in the peri-nasal area (H and E, original magnifications, ×10). (a) Island of basaloid cell with peripheral palisading and keratinocyte formation and horn cyst within the dermis, (b) basaloid cell origin from the epidermis with stromal retraction
Figure 1: Numerous skin-colored or pinkish, papules and nodules on the peri-nasal and chin areas along with a ulcerated nodule in the peri-nasal area and an, ulcerated, severely pruritic lesion on the forehead (highlighted with arrows)
areas. In the peri‑nasal area, a solitary, 4 cm‑sized, ulcerated nodule with telangiectasiae was also detected. In addition, a 4 × 3 cm, ulcerated, severely pruritic lesion was noted on her forehead [Figure 1]. No areas of hypopigmentation were found on the skin lesions. The patient also denied ocular and skeletal problems. Dermatologic examination of the rest of her body was unremarkable. The patient had no significant underlying medical disease and had received no medications or herbal supplements. Biopsy from asymptomatic, non‑ulcerated lesions in the peri‑nasal area showed dermally located islands of basaloid cells with peripheral palisading, abortive hair follicle and keratinous cysts lined by squamous epithelium along with increased fibroblastic cells and stromal fibrosis [Figure 2a]. Excisional biopsy of the ulcerated skin lesion in the peri‑nasal area [Figure 2b] revealed a neoplasm composed of nests of basaloid cells that originated from the overlying epidermis along with stromal retraction. In view of the patient's history and clinical presentation, the histopathology was suggestive of a basal cell carcinoma. Immunohistochemical staining for three immunomarkers including CD10, CD34 and bcl‑2 was performed on the two different skin lesions suspected to be trichoepithelioma and basal cell carcinoma. CD10 and bcl‑2 markers were undetectable on the trichoepithelioma. By contrast, bcl‑2 diffusely stained tumor nests and CD10 was detected in the periphery of basaloid cells of the lesion suspected to be basal cell carcinoma. In addition, CD34 stained neither the trichoepithelioma nor basal cell carcinoma [Figure 3]. 350
The patient had 6 sons and 2 daughters. Two out of the six sons developed similar tiny dome‑shaped lesions on their faces and forehead at ages 34 and 40 years that had been surgically excised. As they lived abroad, we had no access to their medical data including histopathology reports. Her other four sons and two daughters were unaffected. Interestingly, three grandsons aged 17, 21 and 25 years were affected with skin lesions that began at the ages 13, 15 and 19 years, respectively and were similar to those of their grandmother except that they did not have basal cell carcinoma. Their general health was good. The histopathology of lesions in the grandsons was suggestive of trichoepithelioma. The pedigree of the patient’s family is depicted in Figure 4. The clinical manifestations, histopathological findings and family history provided confirmation of the diagnosis of multiple familial trichoepitheliomas. Solitary rather than multiple familial trichoepitheliomas usually share microscopic features with basal cell carcinoma especially in small biopsies.[2] Several histopathological features suggesting a diagnosis of trichoepitheliomas over basal cell carcinoma have been described such as fibrocytic loss of stroma, aggregations with smooth borders, granulomatous inflammation, monomorphic nuclei and papillary mesenchymal bodies.[3] In the present case, histopathological findings (nests of basaloid cells originating from the overlying epidermis with stromal retraction) along with clinical manifestations (ulceration, telangiectasias and peripheral rolled edges) of the skin lesion at the peri‑nasal area were in favor of basal cell carcinoma. Genetic mutations such as those in the cylindromatosis tumor suppressor gene (CYLD) have been associated with multiple familial trichoepitheliomas. Brooke‑Spiegler syndrome, characterized by different combinations of inherited adnexal neoplasms including multiple trichoepitheliomas, cylindromas and spiradenomas, is also linked to the CYLD gene. This
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
Letters to the Editor
a
b
c
d
e
f
Figure 3: Immunohistochemical staining for CD10, CD34 and bcl-2 on two different skin lesions suspected of trichoepitheliomas (a-c) and basal cell carcinoma (d-f). Original magnifications, ×4
Figure 4: Pedigree of the patient’s family. Males and females are indicated by squares and circles, respectively. The patient (grandmother) is identified by the arrow. Probable involvement of the patient’s parents and siblings with similar skin lesions (trichoepitheliomas) was unknown. The patient’s husband and his family including the parents and the brother were unaffected
finding suggests that cylindromas, spiradenomas and multiple familial trichoepitheliomas are phenotypic variations of a single genetic defect.[4] Unfortunately, genetic analyses were not carried out for any members of our reported family including the grandmother, her offspring and grandchildren. However, since cylindromas and/or spiradenomas were not seen in the biopsies of our patients, Brooke‑Spiegler syndrome is unlikely. Immunohistochemical staining technique may also help to distinguish between basal cell carcinoma and multiple familial trichoepitheliomas using antibodies against a number of immunomarkers such as CD34,
bcl‑2, androgen receptor, transforming growth factor‑β and CD10.[2] The diffuse pattern of bcl‑2 staining in our patient’s basal cell carcinoma was in accordance with previous reports.[5] However, a study has questioned the reliability of bcl‑2 in distinguishing multiple familial trichoepitheliomas from basal cell carcinoma.[6] It has been reported that CD10 stains the basaloid cells in basal cell carcinoma while it stains the stroma in multiple familial trichoepitheliomas and may be a useful immunohistochemical marker in differentiating these two entities.[7] In our case, only the peripheral basaloid cells stained strongly with CD10 in the basal cell carcinoma while staining was completely undetectable in the
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
351
Letters to the Editor
trichoepitheliomas. Lack of CD34 staining in both lesions was in contrast to the study conducted by Illueca et al.[8] that reported CD34 expression in multiple familial trichoepitheliomas but not in basal cell carcinoma. Taken together, as in other reports,[9,10] the immunomarkers used in our patient were not very helpful in differentiating these two conditions. Immunostaining with relatively novel markers such as androgen receptor, transforming growth factor‑β, p75 neurotrophin receptor and pleckstrin homology‑like domain, family A, member 1, (not currently available in our laboratory) may be more useful in this regard. Trichoepitheliomas can undergo transformation to malignant neoplasms such as basal cell carcinoma.[1] According to Pincus et al. (2008), six English language reports have appeared from 1959 to 2008 describing eleven patients who developed this malignant neoplasm from multiple familial trichoepitheliomas. Cases of sporadic trichoepitheliomas associated with basal cell carcinoma have also been reported. In four of the above reports, patients presented when the lesions started to bleed and/or ulcerate.[9] Interestingly, one of our patients (the grandmother) sought medical attention because of ulceration and pruritus in a lesion. The history, clincal features, histopathological and immunohistochemistry findings were suggestive of the evolution of basal cell carcinoma directly from trichoepithelioma in our case. Clinicians should examine these patients carefully and be vigilant about any rapid growth or ulceration in the pre‑existing lesions that may indicate malignant transformation.[9]
Mohammad Ali Mapar, Nastaran Ranjbari1, Nasim Afshar, Iman Karimzadeh2, Amin Karimzadeh Departments of Dermatology, and 1Pathology, Imam Khomeini Hospital, Jondishapur University of Medical Sciences, Ahvaz, Iran, 2 Department of Clinical Pharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran Address for correspondence: Dr. Amin Karimzadeh, Department of Dermatology, Imam Khomeini Hospital, Jondishapur University of Medical Sciences, Ahvaz, Iran. E‑mail: [email protected]
REFERENCES 1. Calonje E. Tumors of the skin appendages. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook’s Textbook of Dermatology. Chichester: Wiley‑Blackwell; 2010. 2. Poniecka AW, Alexis JB. An immunohistochemical study of basal cell carcinoma and trichoepithelioma. Am J Dermatopathol 1999;21:332‑6. 3. Ackerman AB, Reddy VB, Soyer HP. Neoplasms with Follicular 352
Differentiation. New York: Ardor Scribendi; 2001. 4. Young AL, Kellermayer R, Szigeti R, Tészás A, Azmi S, Celebi JT. CYLD mutations underlie Brooke‑Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes. Clin Genet 2006;70:246‑9. 5. Verhaegh ME, Arends JW, Majoie IM, Hoekzema R, Neumann HA. Transforming growth factor‑beta and bcl‑2 distribution patterns distinguish trichoepithelioma from basal cell carcinoma. Dermatol Surg 1997;23:695‑700. 6. Abdelsayed RA, Guijarro‑Rojas M, Ibrahim NA, Sangueza OP. Immunohistochemical evaluation of basal cell carcinoma and trichepithelioma using Bcl‑2, Ki67, PCNA and P53. J Cutan Pathol 2000;27:169‑75. 7. Heidarpour M, Rajabi P, Sajadi F. CD10 expression helps to differentiate basal cell carcinoma from trichoepithelioma. J Res Med Sci 2011;16:938‑44. 8. Illueca C, Monteagudo C, Revert A, Llombart‑Bosch A. Diagnostic value of CD34 immunostaining in desmoplastic trichilemmoma. J Cutan Pathol 1998;25:435‑9. 9. Pincus LB, McCalmont TH, Neuhaus IM, Kasper R, Oh DH. Basal cell carcinomas arising within multiple trichoepitheliomas. J Cutan Pathol 2008;35 Suppl 1:59‑64. 10. Arits AH, Parren LJ, van Marion AM, Sommer A, Frank J, Kelleners‑Smeets NW. Basal cell carcinoma and trichoepithelioma: A possible matter of confusion. Int J Dermatol 2008;47 Suppl 1:13‑7. Access this article online Quick Response Code:
Website: www.ijdvl.com DOI: 10.4103/0378-6323.136924 PMID: *****
Panniculitis‑polyarthritis‑ pancreatitis syndrome Sir, Pancreatic panniculitis is a rare variant of panniculitis characterized by subcutaneous fat necrosis that affects 0.3‑3% of patients across a range of different pancreatic disorders. Skin lesions are the presenting feature in about 40% of pancreatic panniculitis and precede the abdominal symptoms by 1‑7 months.[1] Clinically, they present with painful, tender, ill‑defined, erythematous to violaceous nodules that may undergo spontaneous ulceration and discharge of an oily brown, viscous material resulting from liquefactive necrosis of adipocytes. These lesions usually involve the lower extremities although they may also appear on the buttocks, trunk, arms and scalp. In addition to the skin, fat necrosis may involve peri‑articular, abdominal and intramedullary adipose tissue. The
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
Copyright of Indian Journal of Dermatology, Venereology & Leprology is the property of Medknow Publications & Media Pvt. Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use.
and breakdown of skin overlyinging a contiguous tubercular focus in a person with low immunity and tuberculosis verrucosa cutis, an exogenous and paucibacillary form occurring after accidental superinfection or autoinoculation or post‑traumatic inoculation with infected sputum occurring in a person with good immunity.[1] Coexistence of these types of cutaneous tuberculosis with tuberculosis verrucosa cutis developing after scrofuloderma in nearby skin was reported previously by Sethuraman et al.,[3]. Müzeyyen et al.,[2] reported a case where tuberculosis verrucosa cutis was located distant from scrofuloderma. Tuberculosis verrucosa cutis coexisting with articular tuberculosis was reported by Marquet et al.,[6] while scrofuloderma overlying the acromio‑clavicular joint was reported by Tan et al.[7] In our patient, two lesions of tuberculosis verrucosa cutis and two lesions of scrofuloderma with underlying joint involvement were seen in different areas of the hands and feet. The co‑existence of multifocal cutaneous tuberculosis of different forms with joint involvement is rare.
Neelakantababu Rasineni, P. Venkata Ramana, Sridevi Kota, Ramesh Kumar Gandikota Department of Dermatology, Venereology and Leprology, Sri Venkateswara Ramnarayan Ruia Government General Hospital, Sri Venkateswara Medical College, Tirupathi, Andhra Pradesh, India Address for correspondence: Dr. Neelakantababu Rasineni, Department of Dermatology, Venereology and Leprology, Sri Venkateswara Ramnarayan Ruia Government General Hospital, Sri Venkateswara Medical College, Tirupathi ‑ 517507, Andhra Pradesh, India. E‑mail: [email protected]
REFERENCES: 1.
2. 3. 4. 5.
Sethi A.Tuberculosis and infections with atypical mycobacteria. In: Goldsmith LA, Katz SI, Gilcherst BA, Paller AS, Leffell DJ, Wolff K, editors. Fitzpatrick’s Dermatology in General Medicine. 8th ed. New York: McGraw‑Hill; 2012. p. 1225‑36. Gönül M, Gül U, Kilic A, Soylu S, Demiriz M, Kubar A. Coexistence of tuberculosis verrucosa cutis with scrofuloderma. Turk J Med Sci 2008;38:495‑9. Sethuraman G, Kaur J, Nag HL, Khaitan BK, Sharma VK, Singh MK. Symmetrical scrofuloderma with tuberculosis verrucosa cutis. Clin Exp Dermatol 2006;31:475‑7. Rajan J, Mathai AT, Prasad PV, Kaviarasan PK. Multifocal tuberculosis verrucosa cutis. Indian J Dermatol 2011;56:332‑4. Martinez SF, Mihalko MJ. Tuberculosis and other unusual infections. In: Canale ST, Beaty JH, editors. Campbell’s Operative Orthopaedics. 11th ed. Philadelphia: Mosby Company; 2008. p. 753‑71.
6. Marquet A, Moya L, Aldanondo I, Muñoz‑Zato E, Carrillo R, Jaén P. Coexistence of tuberculosis verrucosa cutis and articular tuberculosis in the same patient. Actas Dermosifiliogr 2006;97:56‑8. 7. Tan WP, Tang MB, Tan HH. Scrofuloderma from the acromioclavicular joint presenting as a chronic ulcer in an immunocompetent host. Singapore Med J 2007;48:e243‑5. Access this article online Quick Response Code:
Website: www.ijdvl.com DOI: 10.4103/0378-6323.136921 PMID: *****
Severely disfiguring multiple familial trichoepitheliomas with basal cell carcinoma Sir, Trichoepitheliomas are benign adnexal neoplasms that originate from hair follicles. It can present as solitary non‑familial or multiple familial forms. Multiple familial trichoepitheliomas is an autosomal dominant disorder characterized by numerous nodules and papules predominantly on the face and occasionally on the scalp.[1] Herein, we describe a rare case of this condition, with severe facial disfigurement, involving 6 members of a family in three generations. In the oldest affected member, one of the lesions evolved into a basal cell carcinoma. A 55‑year‑old, rural housewife of Arabian descent presented with slowly progressive facial skin lesions since 37 years. She had noticed her skin lesions at the age of 18 years and they gradually increased in size and number. Although she had sought no medical advice for her asymptomatic lesions during these years (due to her low socio‑economic status), her disfigured face resulted in social isolation. As one of her skin lesions became pruritic and ulcerated recently, she sought medical attention. Physical examination revealed numerous painless, round‑to‑oval, discrete and/or confluent, soft and firm, skin‑colored or pinkish, papules and nodules ranging from 1 to 5 cm in size. These lesions covered the whole face but were predominantly clustered on her peri‑nasal and chin
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
349
Letters to the Editor
a
b
Figure 2: Biopsy of the lesion in the peri-nasal area (H and E, original magnifications, ×10). (a) Island of basaloid cell with peripheral palisading and keratinocyte formation and horn cyst within the dermis, (b) basaloid cell origin from the epidermis with stromal retraction
Figure 1: Numerous skin-colored or pinkish, papules and nodules on the peri-nasal and chin areas along with a ulcerated nodule in the peri-nasal area and an, ulcerated, severely pruritic lesion on the forehead (highlighted with arrows)
areas. In the peri‑nasal area, a solitary, 4 cm‑sized, ulcerated nodule with telangiectasiae was also detected. In addition, a 4 × 3 cm, ulcerated, severely pruritic lesion was noted on her forehead [Figure 1]. No areas of hypopigmentation were found on the skin lesions. The patient also denied ocular and skeletal problems. Dermatologic examination of the rest of her body was unremarkable. The patient had no significant underlying medical disease and had received no medications or herbal supplements. Biopsy from asymptomatic, non‑ulcerated lesions in the peri‑nasal area showed dermally located islands of basaloid cells with peripheral palisading, abortive hair follicle and keratinous cysts lined by squamous epithelium along with increased fibroblastic cells and stromal fibrosis [Figure 2a]. Excisional biopsy of the ulcerated skin lesion in the peri‑nasal area [Figure 2b] revealed a neoplasm composed of nests of basaloid cells that originated from the overlying epidermis along with stromal retraction. In view of the patient's history and clinical presentation, the histopathology was suggestive of a basal cell carcinoma. Immunohistochemical staining for three immunomarkers including CD10, CD34 and bcl‑2 was performed on the two different skin lesions suspected to be trichoepithelioma and basal cell carcinoma. CD10 and bcl‑2 markers were undetectable on the trichoepithelioma. By contrast, bcl‑2 diffusely stained tumor nests and CD10 was detected in the periphery of basaloid cells of the lesion suspected to be basal cell carcinoma. In addition, CD34 stained neither the trichoepithelioma nor basal cell carcinoma [Figure 3]. 350
The patient had 6 sons and 2 daughters. Two out of the six sons developed similar tiny dome‑shaped lesions on their faces and forehead at ages 34 and 40 years that had been surgically excised. As they lived abroad, we had no access to their medical data including histopathology reports. Her other four sons and two daughters were unaffected. Interestingly, three grandsons aged 17, 21 and 25 years were affected with skin lesions that began at the ages 13, 15 and 19 years, respectively and were similar to those of their grandmother except that they did not have basal cell carcinoma. Their general health was good. The histopathology of lesions in the grandsons was suggestive of trichoepithelioma. The pedigree of the patient’s family is depicted in Figure 4. The clinical manifestations, histopathological findings and family history provided confirmation of the diagnosis of multiple familial trichoepitheliomas. Solitary rather than multiple familial trichoepitheliomas usually share microscopic features with basal cell carcinoma especially in small biopsies.[2] Several histopathological features suggesting a diagnosis of trichoepitheliomas over basal cell carcinoma have been described such as fibrocytic loss of stroma, aggregations with smooth borders, granulomatous inflammation, monomorphic nuclei and papillary mesenchymal bodies.[3] In the present case, histopathological findings (nests of basaloid cells originating from the overlying epidermis with stromal retraction) along with clinical manifestations (ulceration, telangiectasias and peripheral rolled edges) of the skin lesion at the peri‑nasal area were in favor of basal cell carcinoma. Genetic mutations such as those in the cylindromatosis tumor suppressor gene (CYLD) have been associated with multiple familial trichoepitheliomas. Brooke‑Spiegler syndrome, characterized by different combinations of inherited adnexal neoplasms including multiple trichoepitheliomas, cylindromas and spiradenomas, is also linked to the CYLD gene. This
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
Letters to the Editor
a
b
c
d
e
f
Figure 3: Immunohistochemical staining for CD10, CD34 and bcl-2 on two different skin lesions suspected of trichoepitheliomas (a-c) and basal cell carcinoma (d-f). Original magnifications, ×4
Figure 4: Pedigree of the patient’s family. Males and females are indicated by squares and circles, respectively. The patient (grandmother) is identified by the arrow. Probable involvement of the patient’s parents and siblings with similar skin lesions (trichoepitheliomas) was unknown. The patient’s husband and his family including the parents and the brother were unaffected
finding suggests that cylindromas, spiradenomas and multiple familial trichoepitheliomas are phenotypic variations of a single genetic defect.[4] Unfortunately, genetic analyses were not carried out for any members of our reported family including the grandmother, her offspring and grandchildren. However, since cylindromas and/or spiradenomas were not seen in the biopsies of our patients, Brooke‑Spiegler syndrome is unlikely. Immunohistochemical staining technique may also help to distinguish between basal cell carcinoma and multiple familial trichoepitheliomas using antibodies against a number of immunomarkers such as CD34,
bcl‑2, androgen receptor, transforming growth factor‑β and CD10.[2] The diffuse pattern of bcl‑2 staining in our patient’s basal cell carcinoma was in accordance with previous reports.[5] However, a study has questioned the reliability of bcl‑2 in distinguishing multiple familial trichoepitheliomas from basal cell carcinoma.[6] It has been reported that CD10 stains the basaloid cells in basal cell carcinoma while it stains the stroma in multiple familial trichoepitheliomas and may be a useful immunohistochemical marker in differentiating these two entities.[7] In our case, only the peripheral basaloid cells stained strongly with CD10 in the basal cell carcinoma while staining was completely undetectable in the
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
351
Letters to the Editor
trichoepitheliomas. Lack of CD34 staining in both lesions was in contrast to the study conducted by Illueca et al.[8] that reported CD34 expression in multiple familial trichoepitheliomas but not in basal cell carcinoma. Taken together, as in other reports,[9,10] the immunomarkers used in our patient were not very helpful in differentiating these two conditions. Immunostaining with relatively novel markers such as androgen receptor, transforming growth factor‑β, p75 neurotrophin receptor and pleckstrin homology‑like domain, family A, member 1, (not currently available in our laboratory) may be more useful in this regard. Trichoepitheliomas can undergo transformation to malignant neoplasms such as basal cell carcinoma.[1] According to Pincus et al. (2008), six English language reports have appeared from 1959 to 2008 describing eleven patients who developed this malignant neoplasm from multiple familial trichoepitheliomas. Cases of sporadic trichoepitheliomas associated with basal cell carcinoma have also been reported. In four of the above reports, patients presented when the lesions started to bleed and/or ulcerate.[9] Interestingly, one of our patients (the grandmother) sought medical attention because of ulceration and pruritus in a lesion. The history, clincal features, histopathological and immunohistochemistry findings were suggestive of the evolution of basal cell carcinoma directly from trichoepithelioma in our case. Clinicians should examine these patients carefully and be vigilant about any rapid growth or ulceration in the pre‑existing lesions that may indicate malignant transformation.[9]
Mohammad Ali Mapar, Nastaran Ranjbari1, Nasim Afshar, Iman Karimzadeh2, Amin Karimzadeh Departments of Dermatology, and 1Pathology, Imam Khomeini Hospital, Jondishapur University of Medical Sciences, Ahvaz, Iran, 2 Department of Clinical Pharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran Address for correspondence: Dr. Amin Karimzadeh, Department of Dermatology, Imam Khomeini Hospital, Jondishapur University of Medical Sciences, Ahvaz, Iran. E‑mail: [email protected]
REFERENCES 1. Calonje E. Tumors of the skin appendages. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook’s Textbook of Dermatology. Chichester: Wiley‑Blackwell; 2010. 2. Poniecka AW, Alexis JB. An immunohistochemical study of basal cell carcinoma and trichoepithelioma. Am J Dermatopathol 1999;21:332‑6. 3. Ackerman AB, Reddy VB, Soyer HP. Neoplasms with Follicular 352
Differentiation. New York: Ardor Scribendi; 2001. 4. Young AL, Kellermayer R, Szigeti R, Tészás A, Azmi S, Celebi JT. CYLD mutations underlie Brooke‑Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes. Clin Genet 2006;70:246‑9. 5. Verhaegh ME, Arends JW, Majoie IM, Hoekzema R, Neumann HA. Transforming growth factor‑beta and bcl‑2 distribution patterns distinguish trichoepithelioma from basal cell carcinoma. Dermatol Surg 1997;23:695‑700. 6. Abdelsayed RA, Guijarro‑Rojas M, Ibrahim NA, Sangueza OP. Immunohistochemical evaluation of basal cell carcinoma and trichepithelioma using Bcl‑2, Ki67, PCNA and P53. J Cutan Pathol 2000;27:169‑75. 7. Heidarpour M, Rajabi P, Sajadi F. CD10 expression helps to differentiate basal cell carcinoma from trichoepithelioma. J Res Med Sci 2011;16:938‑44. 8. Illueca C, Monteagudo C, Revert A, Llombart‑Bosch A. Diagnostic value of CD34 immunostaining in desmoplastic trichilemmoma. J Cutan Pathol 1998;25:435‑9. 9. Pincus LB, McCalmont TH, Neuhaus IM, Kasper R, Oh DH. Basal cell carcinomas arising within multiple trichoepitheliomas. J Cutan Pathol 2008;35 Suppl 1:59‑64. 10. Arits AH, Parren LJ, van Marion AM, Sommer A, Frank J, Kelleners‑Smeets NW. Basal cell carcinoma and trichoepithelioma: A possible matter of confusion. Int J Dermatol 2008;47 Suppl 1:13‑7. Access this article online Quick Response Code:
Website: www.ijdvl.com DOI: 10.4103/0378-6323.136924 PMID: *****
Panniculitis‑polyarthritis‑ pancreatitis syndrome Sir, Pancreatic panniculitis is a rare variant of panniculitis characterized by subcutaneous fat necrosis that affects 0.3‑3% of patients across a range of different pancreatic disorders. Skin lesions are the presenting feature in about 40% of pancreatic panniculitis and precede the abdominal symptoms by 1‑7 months.[1] Clinically, they present with painful, tender, ill‑defined, erythematous to violaceous nodules that may undergo spontaneous ulceration and discharge of an oily brown, viscous material resulting from liquefactive necrosis of adipocytes. These lesions usually involve the lower extremities although they may also appear on the buttocks, trunk, arms and scalp. In addition to the skin, fat necrosis may involve peri‑articular, abdominal and intramedullary adipose tissue. The
Indian Journal of Dermatology, Venereology, and Leprology | July-August 2014 | Vol 80 | Issue 4
Copyright of Indian Journal of Dermatology, Venereology & Leprology is the property of Medknow Publications & Media Pvt. Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use.
