Journal Information
Vol. 45. Issue 8.
Pages 408-410 (August 2009)
Share
Share
Download PDF
More article options
Vol. 45. Issue 8.
Pages 408-410 (August 2009)
Case report
Full text access
Familial Pulmonary Fibrosis in 2 Mexican Sisters With Hermansky-Pudlak Syndrome
Fibrosis pulmonar familiar en 2 hermanas mexicanas con síndrome de Hermansky-Pudlak
Visits
4790
Ana C. Zamoraa,
Corresponding author
zamora72@gmail.com

Corresponding author.
, Delfino Alonso-Martínezb, Lourdes Barreraa, Felipe Mendozaa, Miguel Gaxiolac, Guillermo Carrillob
a Laboratorio de Fibrosis Pulmonar, Inmunoquímica, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, México DF, México
b Laboratorio de Fibrosis Pulmonar, Fibrosis Pulmonar, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, México DF, México
c Departamento de Morfología, Fibrosis Pulmonar, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, México DF, México
This item has received
Article information
Abstract

Hermansky-Pudlak syndrome is an autosomal recessive disorder commonly found in individuals of Puerto Rican ancestry. We present 2 cases of familial pulmonary fibrosis in 2 Mexican sisters with Hermansky-Pudlak syndrome. Pulmonary fibrosis was biopsy-proven in 1 of the patients. This report shows that Hermansky-Pudlak syndrome may occur in individuals of Mexican ancestry.

Keywords:
Interstitial lung disease
Type 2 pneumocytes degeneration
Usual interstitial pneumonia
Resumen

El síndrome de Hermansky-Pudlak (SHP) es una enfermedad autosómica recesiva que comúnmente se presenta en latinos de ascendencia puertorriqueña. Presentamos 2 casos clínicos de fibrosis pulmonar familiar en 2 hermanas mexicanas con SHP. La fibrosis pulmonar se confirmó por biopsia en una paciente. Esta comunicación demuestra que el SHP puede aparecer en población mexicana.

Palabras clave:
Enfermedad pulmonar intersticial
Degeneración de neumocitos tipo 2
Neumonía intersticial usual
Full text is only aviable in PDF
References
[1.]
D.M. Pierson, D. Ionescu, G. Qing, A.M. Yonan, K. Parkinson, T.C. Colby, et al.
Pulmonary fibrosis in Hermansky-Pudlak syndrome. A case report and review.
Respiration, 73 (2006), pp. 382-395
[2.]
F. Hermansky, P. Pudlak.
Albinism associated with hemorrhagic diathesis and nusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies.
Blood, 14 (1959), pp. 162-169
[3.]
C.J. Witkop, M. Nunez Babcock, G.H. Rao, F. Gaudier, C.G. Summers, F. Shanahan, et al.
Albinism and Hermansky-Pudlak syndrome in Puerto Rico.
Bol Asoc Med P R, 82 (1990), pp. 333-339
[4.]
J. Oh, L. Ho, S. Ala-Mello, D. Amato, L. Armstrong, S. Bellucci, et al.
Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity.
Am J Hum Genet, 62 (1998), pp. 593-598
[5.]
K.U. Schallreuter, E. Frenk, L.S. Wolfe, C.J. Witkop, J.M. Wood.
Hermansky-Pudlak syndrome in a Swiss population.
Dermatology, 187 (1993), pp. 248-256
[6.]
B. Richmond, M. Huizing, J. Knapp, A. Koshoffer, Y. Zhao, W.A. Gahl, et al.
Melanocytes derived from patients with Hermansky-Pudlak Syndrome types 1, 2, and 3 have distinct defects in cargo trafficking.
J Invest Dermatol, 124 (2005), pp. 420-427
[7.]
M. Huizing, W.A. Gahl.
Disorders of vesicles of lysosomal lineage: the Hermansky-Pudlak syndromes.
Curr Mol Med, 2 (2002), pp. 451-467
[8.]
S.H. Guttentag, A. Akhtar, J.Q. Tao, E. Atochina, M.E. Rusiniak, R.T. Swank, et al.
Defective surfactant secretion in a mouse model of Hermansky-Pudlak syndrome.
Am J Respir Cell Mol Biol, 33 (2005), pp. 14-21
[9.]
Y. Nakatani, N. Nakamura, J. Sano, Y. Inayama, N. Kawano, S. Yamanaka, et al.
Interstitial pneumonia in Hermansky-Pudlak syndrome: significance of florid foamy swelling/degeneration (giant lamellar body degeneration) of type-2 pneumocytes.
Virchows Arch, 437 (2000), pp. 304-313
[10.]
X. Tang, S. Yamanaka, Y. Miyagi, Y. Nagashima, Y. Nakatani.
Lung pathology of pale ear mouse (model of Hermansky-Pudlak syndrome 1) and beige mouse (model of Chediak-Higashi syndrome): severity of giant lamellar body degeneration of type II pneumocytes correlates with interstitial inflammation.
Pathol Int, 55 (2005), pp. 137-143
[11.]
A.Q. Thomas, K. Lane, J. Phillips III, M. Prince, C. Markin, M. Speer, et al.
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred.
Am J Respir Crit Care Med, 165 (2002), pp. 1322-1328
[12.]
J.A. Whitsett.
Genetic basis of familial interstitial lung disease: misfolding or function of surfactant protein C?.
Am J Respir Crit Care Med, 165 (2002), pp. 1201-1202
[13.]
M. Dong, J.P. Bridges, K. Apsley, Y. Xu, T.E. Weaver.
ERdj4 and ERdj5 are required for endoplasmic reticulum-associated protein degradation of misfolded surfactant protein C.
Mol Biol Cell, 19 (2008), pp. 2620-2630
[14.]
L.M. Nogee, A.E. Dunbar III, S.E. Wert, F. Askin, A. Hamvas, J.A. Whitsett.
A mutation in the surfactant protein C gene associated with familial interstitial lung disease.
N Engl J Med, 344 (2001), pp. 573-579
[15.]
V. Thomas de Montpréville, S. Mussot, E. Dulmet, P. Dartevelle.
Pulmonary fibrosis in Hermansky-Pudlak syndrome is not fully usual.
Ann Pathol, 26 (2006), pp. 445-449
[16.]
K.R. Flaherty, E.L. Thwaite, E.A. Kazerooni, B.H. Gross, G.B. Toews, T.V. Colby, et al.
Radiological versus histological diagnosis in UIP and NSIP: survival implications.
Thorax, 58 (2003), pp. 143-148
Copyright © 2009. Sociedad Española de Neumología y Cirugía Torácica
Archivos de Bronconeumología
Article options
Tools

Are you a health professional able to prescribe or dispense drugs?